FDA NDC Directory · JSON-LD · Markdown

prednisone

NDC 68788-8166 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePREDNISONE
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208412
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20220408
Package count9

External sources

Source: openFDA. Public-domain (CC0).