FDA NDC Directory · JSON-LD · Markdown

Amcinonide

NDC 51672-4060 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076367
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsAMCINONIDE (1 mg/g)
Marketing started20030319
Package count3

External sources

Source: openFDA. Public-domain (CC0).