Prescription Drug Marketing Act of 1987

Summary

Prescription Drug Marketing Act of 1987 - Amends the Federal Food, Drug, and Cosmetic Act to permit only the U.S. manufacturer of a drug to reimport such drug into the United States. Prohibits the sale of prescription drug samples. Prohibits the resale of any drug in bulk, except as specified. Permits the distribution of samples only to practitioners licensed to prescribe such drugs. Requires such practitioners to return a receipt for such drug samples to the manufacturers to be kept and made available to Federal and State officials. Requires drug wholesalers to provide drug purchasers with a statement identifying each sale of the drug. Directs the Secretary of Health and Human Services to issue licensing standards for drug wholesalers. Sets forth criminal penalties for violations of this Act.

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Documents

4 official files

• Public Law (PDF)

  Public Law · EN · 23 April 1988

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• Passed House amended

  summary · EN · 4 May 1987

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• Reported to House with amendment(s)

  summary · EN · 30 April 1987

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• Introduced in House

  summary · EN · 24 February 1987

  Open at official source

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