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Tretinoin

NDC 70771-1933 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218560
Dosage form / routeCREAM · TOPICAL
Active ingredientsTRETINOIN (.25 mg/g)
Marketing started20261001
Package count2

External sources

Source: openFDA. Public-domain (CC0).