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To amend the Federal Food, Drug, and Cosmetic Act to protect and strengthen the drug supply chain in the United States by closing several statutory gaps in the penalty provisions of such Act that apply to drug diversion and counterfeiting.

USA115th CongressHR-2376| House 
| Updated: 5/5/2017
Leonard Lance

Leonard Lance

Republican Representative

New Jersey

Cosponsors (3)
Michael C. Burgess (Republican)Debbie Dingell (Democratic)Gene Green (Democratic)

Health Subcommittee, Energy and Commerce Committee

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Drug Diversion and Counterfeit Crackdown Act of 2017 This bill makes it illegal except in cases of a drug shortage to import into the United States prescription drugs manufactured outside the United States and intended by the manufacturer or labeled to be marketed outside the United States. The bill establishes a penalty for knowingly dispensing or selling a counterfeit drug.
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Timeline
May 4, 2017
Introduced in House
May 4, 2017
Referred to the House Committee on Energy and Commerce.
May 5, 2017
Referred to the Subcommittee on Health.
  • May 4, 2017
    Introduced in House


  • May 4, 2017
    Referred to the House Committee on Energy and Commerce.


  • May 5, 2017
    Referred to the Subcommittee on Health.

Health

Related Bills

  • HR 115-2430: FDA Reauthorization Act of 2017
  • S 115-934: FDA Reauthorization Act of 2017
Consumer affairsDrug safety, medical device, and laboratory regulationDrug trafficking and controlled substancesFraud offenses and financial crimesManufacturing

To amend the Federal Food, Drug, and Cosmetic Act to protect and strengthen the drug supply chain in the United States by closing several statutory gaps in the penalty provisions of such Act that apply to drug diversion and counterfeiting.

USA115th CongressHR-2376| House 
| Updated: 5/5/2017
Drug Diversion and Counterfeit Crackdown Act of 2017 This bill makes it illegal except in cases of a drug shortage to import into the United States prescription drugs manufactured outside the United States and intended by the manufacturer or labeled to be marketed outside the United States. The bill establishes a penalty for knowingly dispensing or selling a counterfeit drug.
View Full Text

Suggested Questions

Get AI-generated questions to help you understand this bill better

Timeline
May 4, 2017
Introduced in House
May 4, 2017
Referred to the House Committee on Energy and Commerce.
May 5, 2017
Referred to the Subcommittee on Health.
  • May 4, 2017
    Introduced in House


  • May 4, 2017
    Referred to the House Committee on Energy and Commerce.


  • May 5, 2017
    Referred to the Subcommittee on Health.
Leonard Lance

Leonard Lance

Republican Representative

New Jersey

Cosponsors (3)
Michael C. Burgess (Republican)Debbie Dingell (Democratic)Gene Green (Democratic)

Health Subcommittee, Energy and Commerce Committee

Health

Related Bills

  • HR 115-2430: FDA Reauthorization Act of 2017
  • S 115-934: FDA Reauthorization Act of 2017
  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Consumer affairsDrug safety, medical device, and laboratory regulationDrug trafficking and controlled substancesFraud offenses and financial crimesManufacturing