# LATANOPROST

NDC: 64980-516
Generic name: latanoprost
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20160901

FDA application: ANDA202442

## 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:"64980-516"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-516
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e25b82a9-1b04-4b40-8472-be107a2a6731