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Tafluprost

NDC 0781-6184 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA209040
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsTAFLUPROST (.0045 mg/.3mL)
Marketing started20221205
Package count1

External sources

Source: openFDA. Public-domain (CC0).