N.M. Admin. Code § 16.19.17.7 - DEFINITIONS
A.
"Board" means the New Mexico board of pharmacy.
B.
"Dangerous Drug" as defined
in the New Mexico Drug, Device and Cosmetic Act, Subsection F of Section
26-1-2 NMSA 1978.
(1) The following substance(s) has(have) been
declared by the N.M. board of pharmacy as "Dangerous Drugs" in accordance with
Section 26-1-18 NMSA 1978 of the Drug,
Device and Cosmetic Act, Section
26-1-18 NMSA 1978 and the Uniform
Licensing Act (Sections
61-1-1 to
61-1-31 NMSA 1978). The board of
pharmacy shall by regulation declare a substance a "dangerous drug" when
necessary and notification shall be sent to all registered pharmacies in the
state within 60 days of the adoption of the regulation. Ephedrine, USP, as
ephedrine hydrochloride or ephedrine sulfate or as any other salt form. Any
compound, mixture, or preparation containing one-half percent or less of
ephedrine or of any salt form of ephedrine is exempt from the above. These
products are exempt because they are approved for sale over the counter (OTC)
without a prescription under federal law, are labeled and marketed in a manner
consistent with the pertinent OTC tentative final or final monograph, are
manufactured and distributed for legitimate medical use in a manner that
reduces or eliminates the likelihood for abuse, and are not marketed,
advertised or labeled for an indication of stimulation, mental alertness,
energy, weight loss, appetite control, or muscle enhancement. These approved
OTC products shall be reported as required of a pseudoephedrine containing
product as defined in Subsection B of
16.19.20.53 NMAC.
(2) A dangerous drug shall be dispensed only
upon the prescription of a practitioner licensed by law to administer or
prescribe such drug.
C.
"Drug storage area" means the area restricted to the storage,
dispensing and distribution of dangerous drugs.
D.
"Research protocol" is the
written documentation stating the objective, method, means of measurement, and
utilization procedure of the dangerous drug.
Notes
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