FDA NDC Directory · JSON-LD · Markdown

PREDNISONE

NDC 70518-4560 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215672
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (10 mg/1)
Marketing started20260202
Package count1

External sources

Source: openFDA. Public-domain (CC0).