NDC 63187-937
Flurbiprofen Sodium 0.3 mg per 1 mL solution/ drops
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Bausch & Lomb Incorporated's NDC 24208-314.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Flurbiprofen: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 0.3 mg per 1 mL
- Approval
- ANDA ANDA074447
- On the market since
- Jan 4, 1995
- Package NDCs
63187-937-25- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2019
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