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Tretinoin

NDC 69238-2323 · HUMAN PRESCRIPTION DRUG · GEL

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217497
Dosage form / routeGEL · TOPICAL
Active ingredientsTRETINOIN (.8 mg/g)
Marketing started20260515
Package count1

External sources

Source: openFDA. Public-domain (CC0).