105 CMR 720.200 - Appendix A

MASSACHUSETTS

LIST OF

INTERCHANGEABLE DRUGS

Department of Public Health regulation 105 CMR 720.050 describes the Massachusetts List of Interchangeable Drugs.

105 CMR 720.050(a) calls for the automatic adoption of all "A" rated drug products listed in the "Approved Drug Products with Therapeutic Equivalence Evaluations" and its supplements as published by the U.S. Food and Drug Administration (FDA), Department of Health and Human Services. This publication is commonly referred to as the "Orange Book". It is reprinted by the U.S. Pharmacopeial Convention Inc. (USP) as Volume III of the USP DI.

105 CMR 720.050(b) allows for the establishment of the Massachusetts Additional List of Interchangeable Drugs (Additional List), and provides the criteria upon which these drug products are approved.

All prescriptions written by generic name can be interchanged if the drug is multi-source. To determine if a prescription written for a brand name drug product is interchangeable in Massachusetts:

1. Look up the drug product by the brand name in the index or by generic name in the "Approved Drug Products with Therapeutic Equivalence Evaluations" ("Orange Book"). The drug products are arranged alphabetically.
2. Compare the dosage form and strength of the drug product prescribed with the dosage form and strength of the same drug product in the "Orange Book".
3. If the same drug product, dosage form and strength has been assigned an "A" rating by FDA and is not listed on the Exception List contained within 105 CMR 720.050, the drug product is interchangeable.
4. If the drug product is not listed in the "Orange Book", refer to 105 CMR 720.050(b), the Massachusetts Additional List of Interchangeable Drugs (Additional List).
5. Look up the drug product by the generic name inthe Additional List. The drug products are arranged alphabetically.
6. Compare the dosage form and strength of the drug product prescribed with the dosage form and strength of the same drug product listed on the Additional List.
7. If the same drug product, dosage form and strength are listed, the drug product is interchangeable.

Copies of the "Approved Drug Products with Therapeutic Equivalence Evaluations" and its supplements ("Orange Book") are available from the:

U.S. Food and Drug Administration

Department of Health and Human Services

Government Printing Office

Washington, D.C. 20402-9371

OPC 6768

(202) 783-3238

and www.fda.gov/cder/drug

Copies of the USP DI (third volume of USP DI is the "Orange Book") are available from:

The United States Pharmacopeial Convention, Inc.,

12601 Twinbrook Parkway

Rockville, MD 20852

(301) 881-0666

Copies of the Massachusetts Additional List of Interchangeable Drug Products (document number 105 CMR 720.000) are available from:

The State House Bookstore Room 116

Boston, MA 02133

(617) 727-2834

and www.magnet.state.ma.us/dph/dcp/Drug Formulary/Drug Interchange

TABLE OF CONTENTS

Foreword

Introduction

Drug Product Problem Reporting Instructions

Exception List

Format of the Additional List

NDA, ANDA, Applicant (name) Changes

Abbreviations

Massachusetts Additional List of Interchangeable Drugs (Alphabetical list of Official (Generic) Drug Names)

Parti al Proprietary Brand Cross-reference

FOREWORD

The Massachusetts List of Interchangeable Drugs, is prepared by the Drug Formulary Commission (DFC) and the Department of Public Health. The DFC is comprised of nine men and women appointed by the Governor for the express purpose of developing a list of those drug products that are safely interchangeable -- that is, equivalent to each other in all significant respects. The DFC was established by M.G.L. c. 17, § 13. This law was enacted with the intent of saving money for consumers ofprescription drugs, since drug products that are marketed under trademark or proprietary names are often available in the generic forms from competing manufacturers at substantially lower prices. M.G.L. c. 112, § 12D mandates prescription forms that allow practitioners to prescribe interchangeable drug products by simply signing the signature line. If a practitioner determines that a brand name drug product should be dispensed, he/she must sign the signature line and write the words "no substitution" in his/her own handwriting in the space provided below the signature line.

The regulations call for the automatic adoptionof "A"rated drugproducts listed in the "Approved Drug Products with Therapeutic Equivalence Evaluations" and its supplements (commonly referred to as the "Orange Book") as published by the U.S. Food and Drug Administration, Department of Healthand Human Services, plus a list of additional drug products, the Massachusetts Additional List of Interchangeable Drugs ("Additional List"), individually reviewed and approved by the DFC and the Department. The regulations provide the criteria upon which the drug products listed on the Additional List are approved for interchange. The regulations also provide the DFC and the Department with the authority to review any "A" rated drug product listed in the "Orange Book" or drug product approved for interchange on the Additional List and delete it from the list of interchangeable drug products if deemed appropriate. Drug products assigned an "A" rating by FDA which are deleted from the Massachusetts List are placed on the Exception List. Drug products listed on the Additional List which are subsequently deleted are removed from the Additional List.

Of the many factors considered by the Commission in determining which drugs to include on the List, equivalent safety and effectiveness are paramount. The Commission reviews evidence on bioequivalence and pharmaceutical equivalence and includes on the List only those drug products determined to be fully interchangeable and whose manufacturers are approved by the U.S. Food and Drug Administration. Practitioners may prescribe any drug that appears on the List with confidence that it is as safe and effective as its brand name counterpart.

The efforts of the Commission in the assessment and evaluation ofdata and the preparationofthe List are to be commended. The Department presents the Massachusetts List of Interchangeable Drugs with pride and with confidence that the List will greatly benefit consumers throughout the Commonwealth.

INTRODUCTION

INTERCHANGEABLE (GENERIC) DRUG LAW

In 1976 the Massachusetts Legislature passed an Act Further Regulating the Establishment of a Formulary of Interchangeable Drug Products (St. 1976, c. 470, § 13), commonly known as the Generic Drug Law. This law, enacted to promote and regulate the use of generic drugs, created the Drug Formulary Commission to develop a list of interchangeable drug products and also required the use of a standard prescription form to encourage practitioners to prescribe generic drugs.

PRESCRIPTION FORM

M.G.L. c. 112, § 12D mandates prescription forms with one signature line. Ifthe prescriber signs the prescription form and writes the words "no substitution" in his/her own handwriting in the space provided below the signature line, the pharmacist must fill the prescription exactly as indicated, with no interchange permitted. However, if the prescriber signs the prescription and does not write "no substitution" under his/her signature, the pharmacist is legally required to dispense a less expensive, equivalent interchangeable drug product listed in the Massachusetts List of Interchangeable Drugs if one is reasonably available.

MASSACHUSETTS LIST OF INTERCHANGEABLE DRUGS

The Massachusetts List of Interchangeable Drugs (MLID) consists of the "A" rated drug products listed in the "Approved Drug Products with Therapeutic Equivalence Evaluations" and its supplements as published by the U.S. Food and Drug Administration, Department of Health and Human Services ("Orange Book") and the Massachusetts Additional List of Interchangeable Drugs (Additional List). The Additional List is developed by the Drug Formulary Commission. The Commission determines drug products to be interchangeable only when they meet certain criteria:

(a) the drug product is available from more than one source, with the same active ingredient in the same dosage form and strength;
(b) its manufacturer is approved by the U.S. Food and Drug Administration (FDA); and
(c) when essential to therapeutic outcome, the manufacturer of the drug has documented clinical evidence of bioequivalence.

The Commission judges that all the drugs included on the MLID meet these standards and are bioequivalent, if essential, based on assessment and evaluation of the U.S. Pharmacopeia and its supplements, other state and hospital formularies, listings of the U.S. Department of Health and Human Services of the FDA, and on the expertise of its members.

The List does not include:

(a) drugs that are protected by patent rights or available from only one source;
(b) many controlled-release and enteric coated drug products since they may not consistently deliver the same quantities of their active ingredients;
(c) those drugs for which the Commission had any significant doubt about safe interchange between manufacturers; and
(d) any drug for which bioequivalence is considered essential but for which bioequivalence has not been demonstrated or an appropriate standard for bioequivalence has not been established.

Bioequivalence is determined to be necessary for a particular drug when bioinequivalence might result in therapeutic failure or hazard to the patient. Bioequivalent drug products do not show a significant difference in the rate and extent of absorption when administered at the same dosage under similar conditions. Drugs that are equivalent in the extent to which they are absorbed into a patient's body that differ in the rate of absorption may be therapeutically equivalent -- having the same medical effect -- either because the rate of absorption is not essential to the attainment of effective body concentrations of the drug, or because the difference in the rate is otherwise considered medically insignificant. Bioequivalence is a primary consideration for those drug products with a narrow therapeutic/toxic dosage range (when variation in the rate orextent of absorption could have a critical effect) where careful determination of the correct dosage and monitoring of the patient is essential to safe and effective use. To determine for which drugs bioequivalence is essential, the Commission relies on expert medical testimony, studies done by the pharmaceutical industry, the knowledge and expertise of the individual members of the Commission, and advice from the FDA.

All drug products manufactured by FDA approved firms are considered safe and effective for their intended use, even if the product has not been included in the MLID. A practitioner may begin a patient's therapy with a drug product from any manufacturer who has been approved by the FDA, even though interchange of the drug once the dosage has been calculated for the individual is not advised.

Several generic drug products are manufactured under the same new drug application (NDA) as the brand name drug products. According to section 1.6 of the Orange Book, drug products with the same NDA are therapeutically equivalent. Massachusetts regulations allow the interchange of these products. Distributors or repackagers of drug products manufactured under the same NDA as the brand name product are not identified in the Orange Book. Pharmacists who may not be able to determine if drug products are interchangeable should contact the manufacturers, distributors or repackagers. In addition the Department maintains an unofficial list of these products.

Information relative to the Interchangeable (Generic) Drug Law may be obtained from the Department of Public Health, Division of Food and Drugs, 305 South Street, Jamaica Plain, MA 02130, telephone number (617) 727-2670, and from the Boards of Registration in Medicine, Dentistry and Pharmacy.

DRUG PRODUCT PROBLEM REPORTING INSTRUCTIONS

Since 1971 the United States Pharmacopeia (USP), in cooperation with various professional associations and the Food and Drug Administration (FDA), has operated the Drug Product Problem Reporting Program. This program can be utilized by pharmacists, physicians, or consumers to report any product problems encountered when using drugs interchanged under the Massachusetts generic drug law. The program is product oriented, and patient identification not requested. Should you prefer to remain anonymous, so indicate to the USP and your name will be withheld from the manufacturer and the FDA. Your participation in reporting problems will help to ensure that the drug products prescribed and dispensed in Massachusetts are of continued high quality.

Reports should be sent to The United States Pharmacopeial Convention, Inc., 12601 Twinbrook Parkway, Rockville, MD 20852, (301) 881-0666. The USP is an impartial, non-governmental organization concerned with drug standards and quality control. After USP receives a report, copies are forwarded to the FDA and to the manufacturer of the product involved. Either the FDA or the manufacturer may act to investigate or correct problems.

EXCEPTION LIST

Orange Book "A" rated drug products not approved for interchange.

There are currently no products designated to be listed on the Exception List.

ADDITIONAL LIST

The Massachusetts Additional List of Interchangeable Drugs (Additional List) has been printed in a format designed to be concise and understandable. Interchangeable drugs are listed alphabetically according to their official (chemical or generic) names, and separate sections in each listing show dosage forms, strengths, FDA approved manufacturers, and categories.

DRUG

Drugs are listed in alphabetical order by their generic names and are printed in capital letters. Drug products containing more than one active ingredient (for example, CODEINE PHOSPHATE, GUAIFENESIN) are listed in the conventional order of ingredients.

Only drug products grouped under single headings are to be interchanged.

DOSAGE FORM

Under the generic names are listed the various multisource dosage forms in which a drug product is available. Abbreviations used for dosage forms and approved manufacturers are found in the front of the Additional List.

Only identical dosage forms and strengths of identical drugs are to be interchanged.

STRENGTH

The approved strengths of the drug products are listed under the heading "Strength(s)." The "strengths" must be read along with the "dosage forms" since any strength shown is available only for the dosage form directly to its left. Dosage strength is in metric units that are sometimes rounded off from apothecary measures, which may introduce slight variations in the strength of certain products. Single ingredient drug product strengths are separated by commas. Combination drug products have a slash separating the strengths of the individual ingredients. If more than one strength of a single component of a combination drug product is approved, they will be separated by commas. For example, the strength of a tablet of aspirin with codeine phosphate is "325mg / 15mg, 30mg, 60mg" which means that the combination is available with 325 milligrams of aspirin and 15, 30, or 60 milligrams of codeine phosphate. Drug products with three or more components have their active ingredients listed individually in parentheses and have slashes separating the strengths of the individual ingredients.

MANUFACTURERS

Next to the heading "Manufacturers" are all approved manufacturers for the drug product in that group, listed by three letter abbreviations in capital letters. (See list of manufacturer abbreviations in front of the Additional List.) Listed manufacturers have met all legal requirements, including compliance with the FDA Good Manufacturing Practices for the production of the drug product indicated. Approved manufacturers hold current new drug applications (NDAs) or abbreviated new drug applications (ANDAs) when required by law.

NDA, ANDA APPLICANT (NAME) CHANGES

Because it is not practical to identify in the Massachusetts Additional List of Interchangeable Drugs (Additional List) each and every product involved when an applicant transfers its entire line of approved drug products to another applicant, or when an applicant changes its name, these transfers and name changes are identified in this section. In addition, the new manufacturers are listed in parenthesis beside the original manufacturer under the Manufacturers' Abbreviations section of the Additional List. Where only partial approved product lines are transferred between applicants, each approved product involved will appear with the manufacturer name change in the Additional List amendment.

Previously listed name changes have been incorporated into the revised Manufacturers' Abbreviations section.

ABBREVIATIONS

The following abbreviations are used in the Massachusetts List of Interchangeable Drugs.

DOSAGE FORMS

aero

aerosol

amp

ampule

cap

capsule

conc

concentrate

e.c.

enteric-coated

elix

elixir

g

gram

Hbr

hydrobromide

HCl

hydrochloride

HC

hydrocortisone

inhl

inhalation

inhl liquid

inhalation liquid

inhl sol

inhalation solution

inj

injection

irr sol

irrigating solution

I.U.

international units

liq

liquid

lot

lotion

mcg

microgram

mEq

milliequivalents

mg

milligram

ml

milliliter

oint

ointment

ophth

ophthalmic

oral gran

oral granules for

reconstitution

oral powder

oral powder for

reconstitution

oral sol

oral solution

pow

powder

sol

solution

SR

sustained release

subl tab

sublingual tablet

supp

suppository

susp

suspension

syr

syrup

tab

tablet

top aero

topical aerosol

top swab

topical swab

U

units

vag

vaginal

MANUFACTURERS' ABBREVIATIONS

3MP

3M Pharmaceutical

AAA

Alpha Therapeutic

ABB

Abbott

ABI

Abic

ABL

Able Laboratories

ACI

ACIC Limited

ACP

Advanced Care Prod.

ADV

Advanced Remedies

AGV

Agvar Chemicals

AKO

Akorn

AKZ

Akzona Inc.

ALC

Alcon Labs

ALL

Allergan Pharmaceuticals

ALI

Alliance Pharmaceutical

ALP

Alpharma

APP

Alphapharm Party

ALT

Altana

ALZ

Alza Corp.

ALR

Alra Laboratories

AMA

Amaric

AMB

Ambix Labs

ACC

American Cyanamid Co.

AHP

American Home Products

ARL

American Regent Labs.

AME

Amersham

AMG

Amgen

AMI

Amide Pharmaceuticals

AMT

American Therapeutics

ANA

Anabolic

ANB

Anbex

ANC

Angus Chemical

ANE

Anesta

ANG

Angelini

APO

Apothecon

APK

Apothekernes

APP

American Pharmaceutical Partners

Inc

ARC

Arcola Labs.

APC

Arcum Pharmaceuticlal Corp.

ARP

Armenpharm

ARM

Armour Pharmaceuticals

ASC

Ascot Hospital Products

ASA

Asta

ASP

Astra Pharmaceuticals LP

ATH

Athena Neurosciences

BAK

Baker Norton

BAN

Banner Pharmacaps

BAP

Barlan Pharmacal

B/I

Boehringer Ingelheim

B/M

Boehringer Mannheim. Ther. Div

BAR

Barr Labs

BAS

Basel Pharmaceuticals

BAT

Bartor

B&L

Bausch & Lomb

BAY

Bayer Corp

BEA

Beach Prod.

B-D

Becton,Dickinson & Co.

BED

Bedford Laboratories

BEL

Bell

BDP

Beta Derm Pharmaceuticals

BER

Berlex

BFA

B.F. Asher

BHC

B.H. Chemicals

BID

Biodevelopment

BIO

Bio Technology General

BIV

Biovail

BLA

Blairex Laboratories

BLO

Block Drug Co.

BLU

Bluline

BRL

Blue Ridge Laboratories

BOC

Bock Pharmacal

BOW

Bowman Pharm.

BMS

Bristol Myers Squibb

BRC

Bracco Diagnostics

BRD

Bradley Pharm.

BRA

Braintree Laboratories

BRI

Bristol-Myers Prod.

BTG

BTG Pharmaceuticals

BVL

Ben-Venue Labs

BYR

Byron Chemical

C&M

C & M Pharmacal

CAD

Cadema Medical Products

CAG

Calgon Corp.

CDC

Carderm Capital

C-P

Chesebrough - Ponds

C-W

Cook - Waite

C/C

Chase Chemical

CSL

Chase Laboratories

C/P

Corvit Pharmaceuticals

CAL

Carlisle

CAM

Camall

CAR

Carnick Labs

CTW

CarterWallace

CEN

Century Pharmaceuticals

CBV

Cetus Ben Venue Therapeutics

CHA

Chamberlin Parenteral Corp.

CHE

Chelsea Laboratories

CHM

Chemed Corp.

CVO

Ciba Vision Ophthalmics

CIR

Circa Pharmaceuticals

CJD

Copanos, J.D.

CLA

Clay - Park

CLO

Clonmel Healthcare

CMB

C.M. Bundy

CMC

Consolidated Midland Corp.

C/T

Controlled Therapeutics

CMP

Carolina Medical Products

CNC

H.R. Cenci

COL

Colgate Palmolive

COM

Combe

CON

Connaught Laboratories

COO

Cooper Labs

COP

Copley Pharmaceutical

CPG

Consolidated Pharmacy Group

CRE

Creighton Products

CUM

Cumberland Swan

CUR

Curatex Pharmaceuticals

CTL

Central Pharmacal

D&G

Davis & Geck

D/L

DPT Laboratories

D-R

Del-Ray Laboratories Inc.

DAN

Danbury Pharmacal

DAR

Darby Group Companies

DEL

Dell

DEP

Deproco

DER

Dermik Laboratories

DES

Deseret Medical

DEY

Deylabs

DHL

DHL Laboratories

DIA

Dial Corp.

DIS

Dista

DMD

Duramed

DMG

D M Graham Laboratories

DOW

Dow Pharmaceutical

DPT

Dupont Pharmaceuticals

DPM

Dupont Merck

DUR

Dura Pharmaceuticals

DUN

Dunhall

DYN

Dynapharm

E/K

Eastman Kodak

EAT

Eaton Medical Corp.

ECR

ECR Pharmaceuticals

ELA

Elan Pharmaceuticals

ELL

Ellis Pharmaceuticals

EMP

EM Pharma

END

Endo

EON

Eon Laboratories

ENQ

Enquay Pharm

ENZ

Enzon

ESR

Elkins-Sinn/AH Robins

ERS

Ersana

ESI

ESI Lederle Generics

ESP

ESI Pharmacal

ETH

Ethicon Inc.

ETX

Ethex

ETK

Ethitek Pharmaceuticals

EVY

Everylife

EZC

E Z EM Co.

FAU

Faulding Pharm. Co.

FER

Ferndale

FRT

Ferrante

FRR

Ferring Labs

FIS

Fisons

FLE

Fleming & Co.

FOR

Forest

FOU

Fougera

FOY

Foy

FRE

Fresenius

G&W

G & W

GAL

Galderma

GEI

Geigy

GEC

Gencon

GED

Genderm

GET

Genentech

GEP

Genpharm

GEV

Geneva

GES

Gensia Sicor Pharmaceuticals Inc

GEZ

Genzyme

GIL

Gilbert Laboratories

GLD

Glades

GLW

GlaxoWellcome

GLE

Glenwood

GLO

Global Pharm.

G/P

Golden Pharms.

GOL

Goldine

GRE

Greenstone

GRI

Griffen,KW

G/L

Gruppo Lepetit

GUA

Guardian

GYM

GYMA Laboratories

GYN

Gynopharm

H-R

Holland-Rantos

HAL

Halsey Labs

HAM

Hamilton Pharmaceuticals

HAN

Hnford GC

HEA

Heather

HEN

Heran Pharmaceutical

HEX

Hexcel Chemical Products

HER

Hermal Pharmaceutical

HIC

Hickam

H/D

Hill Dermaceuticals

HIR

Hirsch Industries

HIT

Hi Tech Pharma

HTP

High Technology Pharmacal

HLC

Halocarbon

HCC

Hoechst Celanese Corp.

HMR

Hoechst Marion Roussell

HOE

Hoechst-Rousel

HOR

Horus Therapeutics

HOY

Hoyt

HUD

Hudson Pharmaceuticals

HUN

Huntington

HYB

Hybritec Inc.

HYG

Hygenics

HYR

Hyrex

IMM

Immunex

IMP

IMP Inc.

ICN

ICN Pharmaceuticals

IMS

International Medication

INP

Interpharm

INV

Invamed, Inc.

INW

Inwood Labs

ICC

Interchem Corp.

ILC

International Latex Corp.

ING

Ingram Pharmaceutical

INH

Inhalon

IOL

Iolab

IOM

Iomed

IPR

IPR Pharm

IVA

IVAX

J&J

Johnson & Johnson

JAC

Jacobus

JAN

Janssen Pharmaceuticals

JER

Jerome Stevens Labs

JRW

Johnson RW

JON

Jones Pharma Inc

KAL

Kalapharm

KBP

Kabi Pharmacia

KEE

Keene

KED

Kendall

KEN

Kenwood

KIN

King Pharmaceuticals

KIR

Kirkman Sales

KNO

Knoll

KPI

Key Pharmaceuticals

KVP

KV Pharmaceutical Co.

L/F

Labs Fournier

L/A

Laboratories Atral

LAF

Lafayette Pharms

LAN

Lannett

LED

Lederle

LEI

Leiras

LEK

Lek Ljubliana

LEM

Lemmon

LEO

Leo Pharms

LIF

Life Labs

LIL

Lilly

LIP

Liposome

LIQ

Liquipharm

LNK

LNK International

LOC

Loch Pharmaceuticals

LOR

Lorex

LOT

Lotus Biochemical

LPI

LPI Holding

LUI

Luitpold

LUS

Lek USA Inc.

LYN

LYNE Laboratories

M/P

Mallinckrodt Pharmaceutical.

MAY

Mayrand

MAT

Matrix Labs

MCG

Mcgaw

MCN

McNeil Consumer Products

MDP

MD Pharmaceuticals

MEA

Mead Johnson

MJN

Mead Johnson Nutritionals

M/R

Medco Research

MVA

Medeva

MEP

Medics Pharmaceuticals

MPI

Medi Physics, Inc.

MAG

Mepha AG

MER

Mericon

MET

Metronic

MGI

MGI Pharma

MID

Midway Medical

MIK

Mikart Laboratories

MIS

Mission Pharmacol

MJP

MJ Pharmaceuticals

MKL

Moore Kirk Labs

MLI

Marchar Laboratories

MLP

Miller Pharmacal

MLX

Milex

MMD

Marion Merrell Dow

MOR

Morton Grove

MCK

Merck & Co.

MSM

Marsam

MSL

Marshall Pharmacal

MTC

Martec

MOV

Mova

MUR

Muro

MUT

Mutual Pharmaceuticals

MYL

Mylan Pharmaceuticals

NEP

Nephron Pharmaceuticals Inc

NEU

Neutrogena

NOR

Norbrook Laboratories

N/W

Norton Waterford

N/N

Novo Nordisk

NEW

Newtron Pharmaceuticals

NHN

Norton HN

NOV

Novocol

NVP

Novopharm Ltd.

NUM

Numark

NYC

Nycomed

NYL

Nylos Trading

ORI

Organon, Inc.

OCL

Oclassen

OHM

OHM Laboratories

OMD

Ohmeda Pharmaceutical

OSA

On Site Azla

ODC

Ormont Drug & Chemical

OPC

Ortho Pharmaceuticals

OPT

Optopic Laboratories Corp.

ORG

Organics

OAP

Otsuka America Pharmaceutical

PAK

Pal-Pak

PAL

Palisades

P/D

Parke Davis

P/I

Plantex/Ikpharm

P/K

Purepac-Kalipharma

P/P

Parmed Pharmaceuticals

PAC

Paco Research

PAD

Paddock Labs

PHD

Pharmaderm

PAN

Panray

PAR

Par

PNL

Parnell

PER

Perrigo

PCE

Pharmachemie

PHC

Pharmics

PHK

Pharmakinetics Labs

PHM

Pharmeral

PHO

Phoenix Labs

PHS

Pharma Serve

PHT

Pharmaton

PFF

Pfeiffer

PFI

Pfizer

P/U

Pharmacia & Upjohn

P/A

Pharmaceutical Association

PIO

Pioneer Pharmaceutical Inc.

PPI

Physicians Products Inc.

PSA

Pharmaceutical Specialist Assoc

POH

Pohl Boskamp

POL

Polymedia

PGP

Prographarm

PRD

Professional Disposables

PRO

Proter Laboratory

PRI

Private Formulations

P&G

Proctor & Gamble

PRV

Pharmavite

PTK

Pharma-Tek

PUF

Purdue Frederick

PUR

Purepac

QUA

Quantum Pharmics Ltd.

QLT

QLT PhototherapeuticsInc.

RAN

Ranbaxy Pharmaceuticals

R/C

Reckitt & Colman

R&C

Reed & Carnrick

R/I

Research Industries

RXP

Rexar Pharmacal

RAC

Rachelle Labs

REN

Ren-Pharm Internatl. Ltd.

RHP

Rhone - Poulenc

RPR

Rhone-Poulenc Rorer

RAH

Robins, A.H.

REX

Rexall/Sundown

RIC

Richlyn Labs

ROC

Roche Labs.

RPF

Roerig/Pfizer

ROA

Roaco

RBP

Roberts Pharmaceutical

ROR

Rorer

ROS

Ross Labs

ROX

Roxane Labs

ROY

Royce Laboratories

RPC

Rosemont Pharmaceutical Corp

RUG

Rugby Labs

S-M

Spencer-Mead

S/W

Sanofi Winthrop

S/L

Schmid Laboratories

SAK

Sankyo

SAV

Savage Labs/Altana

SAN

Sandoz

SCE

Scherer, R.P.

SPI

Schein Pharmaceutical, Inc.

SCH

Schering Corporation

S/P

Schering/Plough

SWZ

Schwarz Pharma

SZG

SchwarzGMBH

SCI

ScinoPharm International

SCS

SCS Pharmaceuticals

SEA

Searle

SER

Serono Laboratories

SEQ

Sequus Pharmaceuticals

SHM

Sherwood Medical

SHI

Shionogi USA

SID

Sidmak Laboratories

SIG

Sigma Tau

SIX

Silarx

SKB

Smith, Kline Beecham

SBH

Sola Barnes Hind

SOL

Solopak Laboratories

SLV

Solvay

SOM

Somerset

SBM

Sorin Biomedics

SDP

Sperti Drug Products

STI

Steifel

STL

Stanlabs Pharmaceutical Co.

STR

Star Pharmaceuticals

STS

Steris Laboratories

STZ

Storz Ophthalmics

SUP

Superpharm

SPP

Suppositoria

SUR

Survival Technology

SYN

Syntex

SYO

Syosset Labs

TAB

Tablicaps

TAG

Tag Pharmaceuticals

TAK

Takeda

TAP

Tap Holdings

TAR

Taro Pharmaceutical

TAY

Taylor Pharmaceuticals

TEC

Technilab

THE

Theratech

THK

Therakos

THA

Thames Phamacol Co. Inc.

TIC

Tican Pharmaceuticals

TOP

Topiderm

T/L

Torch Laboratories

TOR

Torigian Lab

UDL

UDL Laboratories

UMD

Unimed

UPJ

Upjohn

USL

Upsher-Smith Labs

VAL

Vale Chemical

VAN

Vangard

VES

Vestal

VIC

Vicks Pharmacy Products

VIN

Vintage

VIR

Viratek

VIS

Vistakon, Inc.

VIV

Vivan Pharmacal

W-A

Wyeth Ayerst

W-C

Warner-Chilcott

WAW

Warner Wellcome

WRR

Warrick Pharm

WEP

WE Pharmaceuticals

WEN

Wendt Laboratories

WPP

West Point Pharma

WES

Westwood Squibb Pharmaceuticals

W-W

West-Ward

W/L

Wharton Labs

WBY

Whitby

WWT

Whiteworth Towne

WAL

Wallace Labs

WAR

Warner-Lambert

WAT

Watson Laboratories

WOC

Wockhardt

XTT

Xttrium Laboratories

YAM

Yamanouchi

YOS

Yoshitomi Laboratories

ZCA

Zeneca

ZGP

Zenith Goldline Pharmaceuticals

MASSACHUSETTS ADDITIONAL LIST OF INTERCHANGEABLE DRUGS

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PARTIAL PROPRIETARY BRAND CROSS-REFERENCE

Generically equivalent drug products in the same strength and dosage form listed in the Additional List are interchangeable if their respective manufacturers are listed for that product. This partial crossreference section does not attempt to list all brand names which are approvedforinterchange. Formost products only one, usually the innovator or most commonly prescribed brand, is listed below for quick reference purposes.

See page 4105 for precise instructions for determining the interchangeability of drug products.

BRAND SEE

(ATROPINE SULFATE, HYOSCINE HBr, HYOSCYAMINE HBr, PHENOBARBITAL)

(THEOPHYLLINE, POTASSIUM IODIDE, ALCOHOL)

ACTIFED ............................................................TRIPROLIDINE HCl, PSEUDOEPHEDRINE HCl

ANDROID..............................................................................METHYLTESTOSTERONE

ANTABUSE DISULFIRAM

AQUAMEPHYTON............................................................................. PHYTONADIONE

AURALGAN......................................................................... BENZOCAINE, ANTIPYRINE

AZO-GANTANOL.................................................... SULFAMETHOXAZOLE, PHENAZOPYRIDINE

AZO-GANTRISIN .......................................................SULFISOXAZOLE PHENAZOPYRIDINE HCl

AZULFADINE ................................................................................. SULFASALAZINE

BENADRYL ............................................................................DIPHENHYDRAMINE HCl

CYANOCOBALAMIN

BICILLIN............................................................................ PENICILLIN G BENZATHINE

BRETHINE ............................................................................. TERBUTALINE SULFATE

CHLOR-TRIMETON............................................................. CHLORPHENIRAMINE MALEATE

COL-BENEMID .................................................................... PROBENECID W/ COLCHICINE

CYCLANDELATE

DECADRON ................................................................................. DEXAMETHASONE

DESQUAM .................................................................................BENZOYL PEROXIDE

DIMETANE DX................................ BROMPHENIRAMINE, DEXTROMETHORPHAN, PSEUDOEPHEDRINE

DIUPRESS......................................................................CHLOROTHIAZIDE W/ RESERPINE

DONNATAL................................................................... ATROPINE SULFATE COMPOUND

DRAMAMINE ...............................................................................DIMENHYDRINATE

DRIXORAL.................................................................................. (product reformulated)

ECONOPRED ......................................................................... PREDNISOLONE ACETATE

ELIXOPHYLLINE KI ......................................................... THEOPHYLLINE, POTASSIUM IODIDE

EMPIRIN W/ CODEINE .........................................................ASPIRIN W/ CODEINE PHOSPHATE

ESTINYL .................................................................................. ETHINYL ESTRADIOL

EXNA. ........................................................................................ BENZTHIAZIDE

FEDAHIST............................................. PSEUDOEPHEDRINE HCl, CHLORPHENIRAMINE MALEATE

GLAUCON ....................................................................................EPINEPHRINE HCl

GRANULEX ............................................................... TRYPSIN, BALSAM PERU, CASTOR OIL

HALOTESTIN .............................................................................FLUOX\YMESTERONE

HYCOMINE..........................................HYDROCODONE BITARTRATE W/ PHENYLPROPANOLAMINE

HYDROPRES ........................................................... HYDROCHLOROTHIAZIDE W/ RESERPINE

ISOPTO CARPINE ............................................................................. PILOCARPINE HCl

ISORDIL TEMBID....................................................................... ISOSORBIDE DINITRATE

ISUPREL .................................................................................. ISOPROTERENOL HCl

KAON. ............................................................................... POTASSIUM GLUCONATE

KENALOG ....................................................................... TRIAMCINOLONE DIACETATE

LARODOPA .........................................................................................LEVODOPA

LEVSIN ............................................................................. L-HYOSCYAMINE SULFATE

LIBRAX........................................................... CHLORDIAZEPOXIDE W/CLIDINIUM BROMIDE

MANDELAMINE ..................................................................METHENAMINE MANDELATE

MEBARAL ................................................................................... MEPHOBARBITAL

MENEST ...............................................................................ESTROGENS, ESTERIFIED

METALONE T.B.A ...................................................................PREDNISOLONE TEBUTATE

MICRONASE ....................................................................................... GLYBURIDE

MAGNESIUM SALICYLATE

NEO-SYNEPHRINE ......................................................................... PHENYLEPHRINE HCl

CHLORAL HYDRATE

PAMELOR .................................................................................NORTRIPTYLINE HCl

PHENERGAN PLAIN ....................................................................... PROMETHAZINE HCl

PONTOCAINE .................................................................................TETRACAINE HCl

PROSED.................................METHENAMINE COMBINATION (METHENAMINE, PHENYLSALICYLATE,

ATROPINE SULFATE, HYOSCYAMINE, BENZOIC ACID METHYLENE BLUE)

PROSTIGMINE .................................................................NEOSTIGMINE METHYLSULFATE

PYRIDIUM ..............................................................................PHENAZOPYRIDINE HCl

QUINAMM ..................................................................................QUININE SULFATE

SALUTENSIN ............................................................... HYDROFLUMETHIAZIDE, RESERPINE

SANOREX.......................................................................................... MAZINDOL

SERAPES.............................................. HYDRALAZINE HCl, HYDROCHLOROTHIAZIDE, RESERPINE

SLO-PHYLLIN GG ................................................................. THEOPHYLLINE, GUAIFENESIN

SLO-PHYLLIN ....................................................... THEOPHYLLINE (NON-SUSTAINED RELEASE)

SSKI. ...................................................................................... POTASSIUM IODIDE

SUDAFED ...............................................................................PSEUDOEPHEDRINE HCl

SYNTHROID .........................................................................LEVOTHYROXINE SODIUM

TENUATE................................................................................ DIETHYLPROPION HCl

TESTOSTERONE

TUINAL ......................................................AMOBARBITAL SODIUM, SECOBARBITAL SODIUM

VASODILAN ..................................................................................... ISOXSUPRINE

Notes

105 CMR 720.200

State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.


No prior version found.