NDC 63323-367
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 |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Polymyxin B: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intrathecal; intravenous
- Strength
- 500000 [USP'U]
- Approval
- ANDA ANDA202766
- On the market since
- Sep 9, 2015
- Package NDCs
63323-367-4163323-367-44- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2022
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