FDA NDC Directory · JSON-LD · Markdown

Bimatoprost

NDC 0781-6206 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA202719
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsBIMATOPROST (.3 mg/mL)
Marketing started20161206
Package count2

External sources

Source: openFDA. Public-domain (CC0).