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Tretinoin

NDC 51672-1395 · HUMAN PRESCRIPTION DRUG · CREAM

Generic nametretinoin
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211645
Dosage form / routeCREAM · TOPICAL
Active ingredientsTRETINOIN (1 mg/g)
Marketing started20190122
Package count2

External sources

Source: openFDA. Public-domain (CC0).