FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 51655-242 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA085161
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20230306
Package count1

External sources

Source: openFDA. Public-domain (CC0).