NDC 0409-0830
Aztreonam 2 g injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira Australia Pty Ltd | Mulgrave, Australia | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilySep 2, 2022 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Aztreonam: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 2 g
- Approval
- ANDA ANDA206517
- On the market since
- Jan 24, 2022
- Package NDCs
0409-0830-010409-0830-11- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2024
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