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Virginia Administrative Code (Last Updated: January 10, 2017) |
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Title 18. Professional and Occupational Licensing |
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Agency 110. Board of Pharmacy |
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Chapter 30. Regulations for Practitioners of the Healing Arts to Sell Controlled Substances |
Section 210. Repackaging of controlled substances; records required; labeling requirements
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Part V. Packaging, Repackaging and Label Standards
A. A licensee repackaging controlled substances shall maintain adequate control records for a period of one year or until the expiration, whichever is greater. The records shall show the name of the controlled substances repackaged, strength, if any, quantity prepared, initials of the licensee supervising the process, the assigned control number, or the manufacturer's or distributor's name and control number, and an expiration date.
B. The controlled substance name, strength, if any, the assigned control number, or the manufacturer's or distributor's name and control number, and an appropriate expiration date determined by the licensee in accordance with USP-NF guidelines shall appear on any subsequently repackaged or reconstituted units.
Historical Notes
Derived from VR530-01-2 § 5.1, eff. May 9, 1990; amended, Volume 08, Issue 13, eff. April 22, 1992; Volume 10, Issue 01, eff. November 3, 1993; Volume 17, Issue 07, eff. January 17, 2001; Volume 22, Issue 10, eff. February 22, 2006.