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prednisone

NDC 64380-835 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePREDNISONE
Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208412
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (2.5 mg/1)
Marketing started20210901
Package count2

External sources

Source: openFDA. Public-domain (CC0).