FDA NDC Directory · JSON-LD · Markdown

prednisone

NDC 51655-068 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePREDNISONE
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209727
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started20220928
Package count2

External sources

Source: openFDA. Public-domain (CC0).