NDC 63323-401
Aztreonam 1 g 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 | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Product details
- Generic drug
- Aztreonam: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 1 g
- Approval
- ANDA ANDA065439
- On the market since
- Nov 5, 2009
- Package NDCs
63323-401-2463323-401-41- Official label
- DailyMed (National Library of Medicine), updated May 6, 2022
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