FDA NDC Directory · JSON-LD · Markdown

PredniSONE

NDC 68071-2509 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA080352
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started20200323
Package count6

External sources

Source: openFDA. Public-domain (CC0).