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Latanoprost

NDC 65862-872 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206519
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsLATANOPROST (50 ug/mL)
Marketing started20190903
Package count1

External sources

Source: openFDA. Public-domain (CC0).