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- Regulations
- Code of Federal Regulations
- Title 21. Food and Drugs
- Chapter I. Food and Drug Administration, Department of Health and Human Services
- Subchapter D. Drugs For Human Use
- Part 341. Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug Products For Over-the-counter Human Use
- Subpart C. Labeling
21 C.F.R. §341.76 - Labeling of bronchodilator drug products
| Cite as | 21 C.F.R. §341.76 |
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Green v. Bdi Pharmaceuticals, 35,291-CA.
- United States
- Court of Appeal of Louisiana (US)
- 31 Octubre 2001
...as reasonably anticipated use. BDI further argued that because its labels comply with Food and Drug Administration regulations, 21 C.F.R. §§ 341.76, 341.78, the sufficiency of the warning is preempted by Federal law, 21 U.S.C. § 379r (a). Finally, BDI argued that not only was Green's defect......