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Tacrolimus

NDC 68462-534 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA210393
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsTACROLIMUS (1 mg/g)
Marketing started20180416
Package count3

External sources

Source: openFDA. Public-domain (CC0).