FDA NDC Directory · JSON-LD · Markdown

PrednisoLONE

NDC 0527-5406 · HUMAN PRESCRIPTION DRUG · SYRUP

Generic namePrednisolone
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040775
Dosage form / routeSYRUP · ORAL
Active ingredientsPREDNISOLONE (15 mg/5mL)
Marketing started20070921
Package count2

External sources

Source: openFDA. Public-domain (CC0).