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Tretinoin

NDC 62332-808 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214590
Dosage form / routeCREAM · TOPICAL
Active ingredientsTRETINOIN (.5 mg/g)
Marketing started20260611
Package count2

External sources

Source: openFDA. Public-domain (CC0).