FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 0591-5052 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA080356
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started19900101
Package count4

External sources

Source: openFDA. Public-domain (CC0).