NDC 68071-4650
Latanoprost 50 ug per 1 mL solution/ drops
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-463.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch & Lomb Incorporated | Tampa, FL, United States | Makes it | Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Latanoprost: every company that makes it
- Form
- solution/ drops
- Strength
- 50 ug per 1 mL
- Approval
- ANDA ANDA201006
- On the market since
- Mar 22, 2011
- Package NDCs
68071-4650-2- Official label
- DailyMed (National Library of Medicine), updated Feb 17, 2021
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