FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 60687-122 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA040256
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (5 mg/1)
Marketing started20150910
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).