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21 U.S.C. § 356-1
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Nearby current sections
- § 355h — Regulation of certain nonprescription drugs that are marketed without an approved drug application
- § 355–1 — Risk evaluation and mitigation strategies
- § 355–2 — Actions for delays of generic drugs and biosimilar biological products
- § 356 — Expedited approval of drugs for serious or life-threatening diseases or conditions
- § 356a — Manufacturing changes
- § 356b — Reports of postmarketing studies
- § 356c — Discontinuance or interruption in the production of life-saving drugs
- § 356c–1 — Annual reporting on drug shortages