NDC 24208-734
Fluorescein Sodium and Benoxinate Hydrochloride 2.6 mg per 1 mL / 4.4 mg per 1 mL solution/ drops
On the label: Bausch & Lomb Incorporated.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alliance Medical Products, Inc. (dba Siegfried Irvine) | Irvine, CA, United States | Makes it | Problems found, fixed voluntarilyNov 7, 2025 · 12 inspections |
Product details
- Generic drug
- Benoxinate and Fluorescein: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 2.6 mg per 1 mL / 4.4 mg per 1 mL
- Approval
- NDA NDA211039
- On the market since
- Mar 20, 2020
- Package NDCs
24208-734-05- Official label
- DailyMed (National Library of Medicine), updated May 12, 2025
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