NDC 68071-1650
Sulfacetamide Sodium and Prednisolone Sodium Phosphate 100 mg per 1 mL / 2.3 mg per 1 mL solution/ drops
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Prednisolone and Sulfacetamide: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 100 mg per 1 mL / 2.3 mg per 1 mL
- Approval
- ANDA ANDA074449
- On the market since
- Dec 29, 1995
- Package NDCs
68071-1650-5- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?