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Tretinoin

NDC 59651-712 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218246
Dosage form / routeGEL · TOPICAL
Active ingredientsTRETINOIN (.1 mg/g)
Marketing started20250113
Package count2

External sources

Source: openFDA. Public-domain (CC0).