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Hydrocortisone Butyrate

NDC 51672-4083 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076842
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsHYDROCORTISONE BUTYRATE (1 mg/g)
Marketing started20041227
Package count5

External sources

Source: openFDA. Public-domain (CC0).