FDA NDC Directory · JSON-LD · Markdown

XELPROS

NDC 47335-317 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Generic namelatanoprost
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA206185
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC TOPICAL
Active ingredientsLATANOPROST (.05 mg/mL)
Marketing started20180912
Package count4

External sources

Source: openFDA. Public-domain (CC0).