FDA NDC Directory · JSON-LD · Markdown

Azelaic Acid

NDC 51672-1389 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210549
Dosage form / routeGEL · TOPICAL
Active ingredientsAZELAIC ACID (.15 g/g)
Marketing started20190823
Package count1

External sources

Source: openFDA. Public-domain (CC0).