FDA NDC Directory · JSON-LD · Markdown

PredniSONE

NDC 63187-243 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA084283
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (50 mg/1)
Marketing started20030314
Package count9

External sources

Source: openFDA. Public-domain (CC0).