NDC 76420-254
Gentamicin Sulfate 3 mg per 1 mL solution/ drops
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-580.
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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Gentamicin: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 3 mg per 1 mL
- Approval
- ANDA ANDA064048
- On the market since
- May 11, 1994
- Package NDCs
76420-254-05- Official label
- DailyMed (National Library of Medicine), updated Jul 19, 2022
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