FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 0378-0642 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA083677
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20200206
Package count3

External sources

Source: openFDA. Public-domain (CC0).