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Tretinoin

NDC 51672-1394 · HUMAN PRESCRIPTION DRUG · CREAM

Generic nametretinoin
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211644
Dosage form / routeCREAM · TOPICAL
Active ingredientsTRETINOIN (.5 mg/g)
Marketing started20190125
Package count2

External sources

Source: openFDA. Public-domain (CC0).