NDC 53002-8690
Sulfacetamide Sodium and Prednisolone Sodium Phosphate 100 mg per 1 mL / 2.3 mg per 1 mL solution/ drops
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-317.
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
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Prednisolone and Sulfacetamide: every company that makes it
- Form
- solution/ drops
- Strength
- 100 mg per 1 mL / 2.3 mg per 1 mL
- Approval
- ANDA ANDA074449
- On the market since
- Dec 29, 1995
- Package NDCs
53002-8690-153002-8690-2- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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