FDA NDC Directory · JSON-LD · Markdown

Prednisone

NDC 60687-145 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA040392
Dosage form / routeTABLET · ORAL
Active ingredientsPREDNISONE (20 mg/1)
Marketing started20151005
Marketing ended20270331
Package count1

External sources

Source: openFDA. Public-domain (CC0).