FDA NDC Directory · JSON-LD · Markdown

PredniSONE

NDC 17856-3722 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAtlantic Biologicals Corps
Marketing categoryAbbreviated NDA (generic) · App ANDA088703
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISONE (5 mg/5mL)
Marketing started19861213
Package count1

External sources

Source: openFDA. Public-domain (CC0).