FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 72189-489 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA208412
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (50 mg/1)
Marketing started20230607
Package count1

External sources

Source: openFDA. Public-domain (CC0).