FDA NDC Directory · JSON-LD · Markdown

prednisone

NDC 51655-541 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePREDNISONE
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208412
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20230519
Package count8

External sources

Source: openFDA. Public-domain (CC0).