NDC 76420-090
Sulfacetamide Sodium 100 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 24208-670.
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
- Sulfacetamide: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA040066
- On the market since
- Dec 28, 1994
- Package NDCs
76420-090-15- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2020
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