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Prednisone

NDC 71205-089 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA040611
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (1 mg/1)
Marketing started20050606
Package count17

External sources

Source: openFDA. Public-domain (CC0).