NDC 0404-9962
Terbutaline Sulfate 1 mg per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Fresenius Kabi, LLC's NDC 63323-665.
Where the pills inside were 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
- Jan 12, 2022
- Package NDCs
0404-9962-01- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2025
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