FDA NDC Directory · JSON-LD · Markdown

PREDNISONE

NDC 68071-2661 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208412
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20210901
Package count6

External sources

Source: openFDA. Public-domain (CC0).