FDA NDC Directory · JSON-LD · Markdown

PredniSONE

NDC 70518-4191 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA084122
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20240930
Package count3

External sources

Source: openFDA. Public-domain (CC0).