NDC 68071-2376
Latanoprost 50 ug per 1 mL solution/ drops
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Somerset Therapeutics, LLC's NDC 70069-421.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Latanoprost Acid: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 50 ug per 1 mL
- Approval
- ANDA ANDA201786
- On the market since
- Dec 3, 2019
- Package NDCs
68071-2376-2- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2026
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