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Tazarotene

NDC 51672-1373 · HUMAN PRESCRIPTION DRUG · CREAM

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208258
Dosage form / routeCREAM · TOPICAL
Active ingredientsTAZAROTENE (1 mg/g)
Marketing started20170403
Package count2

External sources

Source: openFDA. Public-domain (CC0).