Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products¶
U.S. Food and Drug Administration. Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products.
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Primes¶
- Boundary Disclosure Card
- In pharmaceuticals, package inserts carry indications, dosage, contraindications, and interactions in every box.
This sourceFinal rule, 71 Fed. Reg. 3922 (Jan. 24, 2006). Mandates that prescription-drug labeling (package inserts) carry indications, dosage, contraindications, and interactions in a fixed order in every box.
- In pharmaceuticals, package inserts carry indications, dosage, contraindications, and interactions in every box.
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