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Tretinoin

NDC 0378-8090 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207955
Dosage form / routeGEL · TOPICAL
Active ingredientsTRETINOIN (.5 mg/g)
Marketing started20181114
Package count1

External sources

Source: openFDA. Public-domain (CC0).