NDC 72266-249
Polymyxin B 500000 [USP'U] injection, powder, lyophilized, for solution
On the label: Fosun Pharma USA Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Fosun Pharma USA Inc. names for other drugs.
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 ANDA207322
- On the market since
- Aug 31, 2023
- Package NDCs
72266-249-0172266-249-10- Official label
- DailyMed (National Library of Medicine), updated May 29, 2025
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