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Prednisone delayed release

NDC 43598-888 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namePrednisone
Labeler / ManufacturerDr. Reddys Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218035
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started20260812
Package count2

External sources

Source: openFDA. Public-domain (CC0).