FDA NDC Directory · JSON-LD · Markdown

Prednisolone

NDC 70404-077 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic namePrednisolone oral
Labeler / ManufacturerTulex Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA219509
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE (15 mg/5mL)
Marketing started20260708
Package count2

External sources

Source: openFDA. Public-domain (CC0).