NDC 53002-9000
Neomycin and Polymyxin B Sulfates and Hydrocortisone 10 mg per 1 mL / 3.5 mg per 1 mL / 10000 [USP'U] per 1 mL suspension/ drops
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-635.
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 |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes the active ingredient | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · relabels it
Product details
- Generic drug
- Hydrocortisone and Neomycin and Polymyxin B: every company that makes it
- Form
- suspension/ drops
- Strength
- 10 mg per 1 mL / 3.5 mg per 1 mL / 10000 [USP'U] per 1 mL
- Approval
- ANDA ANDA064065
- On the market since
- Aug 28, 1996
- Package NDCs
53002-9000-1- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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