Nev. Admin. Code § 639.Sec. 4.6 - NEW
1. A pharmacist, pharmaceutical technician or
dispensing practitioner may add flavoring to an oral drug product at the
request of a patient or a legal guardian of the patient, as applicable. A
pharmacist, pharmaceutical technician or dispensing practitioner who adds
flavoring to an oral drug product pursuant to this subsection shall:
(a) Make a record contemporaneous with the
completion of the mixture, including, without limitation, the ingredients of
the oral drug product;
(b) Ensure
that the flavor additive does not compromise the stability, safety or efficacy
of the dispensed oral drug product; and
(c) Assign the applicable beyond-use date to
the oral drug product pursuant to chapter 795 of the United States
Pharmacopeia - National Formulary, as adopted by reference in
paragraph (b) of subsection 1 of NAC
639.670.
2. Except as otherwise provided in paragraph
(c) of subsection 1, a pharmacist, pharmaceutical technician or dispensing
practitioner is not required to comply with the compounding standards
established in the publications and standards adopted by reference in
subsection 1 of NAC
639.670 when he or she adds
flavoring to an oral drug product pursuant to subsection 1 of this
section.
Notes
NRS 639.070
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