N.M. Admin. Code § 13.10.13.10 - PRESCRIPTION DRUGS
A. No
MHCP that provides coverage for prescription drugs as a basic or supplemental
health care service or pursuant to inpatient, urgent, or emergency medical
services shall limit or exclude coverage for any drug approved by the FDA on
the basis that the drug has not been approved by the FDA for the treatment of
the particular indication for which the drug has been prescribed, provided
that:
(1) the drug has been recognized as
safe and effective for the treatment of that indication in one or more of the
standard medical reference compendia, including the "AMA drug evaluations," the
"American hospital formulary service drug information," and "drug information
for the healthcare provider," or
(2) as provided for cancer clinical trials,
pursuant to Section
59A-22-43 NMSA.
B. Coverage of a drug includes
medically necessary services associated with the administration of the drug
provided that such services would not be otherwise excluded from
coverage.
C. Coverage of a drug
includes coverage for prescription contraceptive drugs or devices, pursuant to
Sections 59A-22-42 and
59A-46-44 NMSA 1978.
D. Nothing in this section requires:
(1) coverage for any drug if the FDA has
determined its use to be contraindicated for the treatment of the particular
indication for which the drug has been prescribed;
(2) coverage for experimental or
investigational drugs not approved for any indication by the FDA; and
(3) reimbursement or coverage for any drug
not included on the drug formulary or list of covered drugs specified in a
managed health care plan, contract, or policy, subject to the exceptions listed
in Subsection D of
13.10.13.10 NMAC.
E. Every MHCP must allow covered
persons to obtain drugs not on the formulary as though the drug were included
in the formulary, based on the type of drug, how the drug is administered, and
the medically necessary services, when the treatment for which the drug is
prescribed is a covered benefit, and when the participating provider in
consultation with the MHCP determines that:
(1) the formulary drug has been or is
reasonably expected to be less effective for the covered person; or
(2) the formulary drug has caused or is
reasonably expected to cause adverse reactions in the covered person.
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.