FDA NDC Directory · JSON-LD · Markdown

Hydrocortisone Butyrate

NDC 68682-271 · HUMAN PRESCRIPTION DRUG · OINTMENT

Generic namehydrocortisone butyrate
Labeler / ManufacturerOceanside Pharmaceuticals
Marketing categoryNew Drug Application (innovator) · App NDA018652
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsHYDROCORTISONE BUTYRATE (1 mg/g)
Marketing started20090901
Package count2

External sources

Source: openFDA. Public-domain (CC0).