LD 576
pg. 5
Page 4 of 6 An Act to Update and Amend the Maine Pharmacy Act Page 6 of 6
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LR 1027
Item 1

 
profile record. As used in this section, "Medicare" means the
Health Insurance for the Aged Act, Title XVIII of the Social
Security Amendments of 1965, as amended.

 
Sec. 14. 32 MRSA §13794, as enacted by PL 1987, c. 710, §5, is
amended to read:

 
§13794. Labeling of prescriptions

 
Every drug dispensed pursuant to prescription, whether for a
legend drug or not, shall must carry on the label the following
information: The the prescription number; the date of filling;
the patient's name; directions for use; the name and strength of
the drug and the amount dispensed, including either the brand
name of the drug or, if a generic and therapeutically equivalent
drug is dispensed, it shall must be in accordance with section
13781; the beyond use date of the drug; the name of the
practitioner prescribing the drug; and the name, address and
telephone number of the pharmacy where the prescription was
compounded and dispensed. For purposes of this section, "beyond
use date" means a date beyond which the contents of the
prescription are not recommended to be used.

 
Sec. 15. Statutory Review Committee

 
1. Establishment. The Commissioner of Professional and
Financial Regulation shall establish a statutory review committee
within 30 days of the effective date of this Act. The size and
composition of the committee is determined by the commissioner,
except that, membership must include a licensed pharmacist in
independent practice, a representative of a corporate pharmacy
chain, a licensed pharmacist working in an institutional setting,
a consumer representative and a representative of prescribing
practitioners. At least one pharmacist member must be a member
of the Board of Pharmacy.

 
2. Charge. The committee is charged with the following
duties:

 
A. To review the current scope of practice for pharmacists,
as set forth in the Maine Revised Statutes, Title 32,
section 13702, subsection 22 and to recommend whether
changes should be made to reflect current professional
practices or prospective professional practices that would
be advantageous to the public. The discussion regarding
scope of practice must include, but is not limited to, drug
or device administration and collaborative practice.

 
B. To review the adequacy of the current regulatory
relationship between the Maine Board of Pharmacy and
institutional pharmacies and propose changes if necessary.


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