# latanoprost

NDC: 68462-944
Generic name: latanoprost
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20241126

FDA application: ANDA218257

## Active ingredients

- LATANOPROST: 50 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-944"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-944
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=821d2ad5-a430-4fd2-8cfd-50b2118b8639