NDC 68462-944
latanoprost 50 ug per 1 mL solution/ drops
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Latanoprost Acid: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 50 ug per 1 mL
- Approval
- ANDA ANDA218257
- On the market since
- Nov 26, 2024
- Package NDCs
68462-944-03- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2025
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