Counterfeit Drug Law and Legal Definition
According to 21 USCS § 321, "counterfeit drug" means a drug which, or the container or labeling of which, without authorization, bears the trademark, trade name, or other identifying mark, imprint, or device, or any likeness thereof, of a drug manufacturer, processor, packer, or distributor other than the person or persons who in fact manufactured, processed, packed, or distributed such drug and which thereby falsely purports or is represented to be the product of, or to have been packed or distributed by, such other drug manufacturer, processor, packer, or distributor.
Legal Definition list
Related Legal Terms
- Abbreviated Drug Application
- Abbreviated New Drug Applications [ANDA]
- Accidental Radiation Occurrence [Food and Drugs]
- Addictive Drug
- Adverse Drug Experience
- AIDS Drug Assistance Programs
- Animal Drug Availability Act
- Animal Drug Product [Food and Drugs]
- Animal Drug User Fee Act of 2003 [ADUFA]
- Anti Counterfeiting Trade Agreement (ACTA)
