FDA NDC Directory · JSON-LD · Markdown

CLOBETASOL PROPIONATE

NDC 59651-732 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075057
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsCLOBETASOL PROPIONATE (.5 mg/g)
Marketing started20230928
Package count4

External sources

Source: openFDA. Public-domain (CC0).