# Latanoprost

NDC: 65862-872
Generic name: Latanoprost
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20190903

FDA application: ANDA206519

## 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:"65862-872"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-872
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19cdfef0-b770-4758-8f59-1769e4b6119c