FDA NDC Directory · JSON-LD · Markdown

PredniSONE Tablets, USP, 5 mg

NDC 72162-2484 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePredniSONE
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA212629
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started20240306
Package count2

External sources

Source: openFDA. Public-domain (CC0).