FDA NDC Directory · JSON-LD · Markdown

PredniSONE

NDC 51655-701 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA087342
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20210419
Package count3

External sources

Source: openFDA. Public-domain (CC0).