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Prednisone delayed release

NDC 74157-019 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namePrednisone
Labeler / ManufacturerINA Pharmaceutics Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA219477
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPREDNISONE (2 mg/1)
Marketing started20251215
Package count1

External sources

Source: openFDA. Public-domain (CC0).