NDC 63323-665
Terbutaline Sulfate 1 mg per 1 mL injection, 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 | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Terbutaline: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA076887
- On the market since
- Mar 10, 2011
- Package NDCs
63323-665-0063323-665-01- Official label
- DailyMed (National Library of Medicine), updated Jul 12, 2022
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