FDA NDC Directory · JSON-LD · Markdown

Hydrocortisone Butyrate

NDC 51672-4061 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076364
Dosage form / routeSOLUTION · TOPICAL
Active ingredientsHYDROCORTISONE BUTYRATE (1 mg/mL)
Marketing started20040114
Package count2

External sources

Source: openFDA. Public-domain (CC0).