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Prednisolone

NDC 23155-927 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameprednisolone oral solution
Labeler / ManufacturerHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040323
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE (15 mg/5mL)
Marketing started20250301
Package count2

External sources

Source: openFDA. Public-domain (CC0).