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Prednisone

NDC 63187-997 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA080356
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started19900101
Package count18

External sources

Source: openFDA. Public-domain (CC0).