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PredniSONE

NDC 55289-330 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA084283
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20030213
Package count3

External sources

Source: openFDA. Public-domain (CC0).