Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements, and Administrative Procedures
hospital-facility · Food and Drug Administration · Rule · Published 1999-12-03 · Effective 2000-12-04 · 64 FR 67720
Document
Document number
99-30954
Federal Register citation
64 FR 67720
CFR reference
21 CFR 203
Type
Rule
Action
Final rule.
Category
hospital-facility
Sub-agency
Food and Drug Administration
Publication date
1999-12-03
Effective date
2000-12-04
HHS docket
Docket Nos. 92N-0297 and 88N-0258
Abstract
The Food and Drug Administration (FDA) is issuing a final rule to set forth procedures and requirements implementing the Prescription Drug Marketing Act of 1987 (PDMA), as modified by the Prescription Drug Amendments of 1992 (PDA) and the FDA Modernization Act of 1997 (the Modernization Act). The final rule sets forth requirements for the reimportation and wholesale distribution of prescription drugs; the sale, purchase, or trade of, or the offer to sell, purchase, or trade, prescription drugs that were purchased by hospitals or health care entities, or donated to charitable organizations; and the distribution of prescription drug samples. FDA is also amending certain sections of the regulations entitled ``Guidelines for State Licensing of Wholesale Prescription Drug Distributors'' to make them consistent with this final regulation. DATES: Submit written comments on the collection of information provisions by February 1, 2000. This regulation is effective December 4, 2000.