Acronym | PDMA |
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Enacted by the | 100th United States Congress |
Citations | |
Public Law | P.L. 100-293 |
Stat. | 102 Stat. 95 |
Codification | |
Legislative history | |
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Major amendments | |
Prescription Drug Amendments of 1992 P.L. 102-353, 106 Stat. 941 | |
Relevant Supreme Court cases | |
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Regulation of therapeutic goods in the United States |
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Prescription drugs Over-the-counter drugs |
Non-governmental organizations
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The Prescription Drug Marketing Act (PDMA) of 1987 (P.L. 100-293, 102 Stat. 95) is a law of the United States federal government. It establishes legal safeguards for prescription drug distribution to ensure safe and effective pharmaceuticals. It's designed to discourage the sale of counterfeit, adulterated, misbranded, subpotent, and expired prescription drugs. It was passed in response to the development of a wholesale sub-market (known as the "diversion market") for prescription drugs.
The PDMA was modified by the Prescription Drug Amendments of 1992 (P.L. 102-353, 106 Stat. 941) on August 26, 1992.
The U.S. Food and Drug Administration (FDA) issued regulations implementing the PDMA in 1990 (21 C.F.R. Part 205) and 1999 (21 C.F.R. Part 203).