NDC 63323-321
Polymyxin B 500000 [USP'U] injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Polymyxin B: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intrathecal; intravenous; ophthalmic
- Strength
- 500000 [USP'U]
- Approval
- ANDA ANDA065372
- On the market since
- Nov 17, 2009
- Package NDCs
63323-321-0263323-321-12- Official label
- DailyMed (National Library of Medicine), updated May 31, 2021
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