FDA NDC Directory · JSON-LD · Markdown

Hydrocortisone Butyrate

NDC 51672-4074 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076654
Dosage form / routeCREAM · TOPICAL
Active ingredientsHYDROCORTISONE BUTYRATE (1 mg/g)
Marketing started20050804
Package count5

External sources

Source: openFDA. Public-domain (CC0).