NDC 59923-615
Terbutaline Sulfate 1 mg per 1 mL injection
On the label: Areva Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| UBI Pharma Inc. | Hukou, Taiwan | Makes it | Problems found, fixed voluntarilyJun 6, 2023 · 4 inspections |
Product details
- Generic drug
- Terbutaline: every company that makes it
- Form
- injection
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA200122
- On the market since
- Oct 4, 2024
- Package NDCs
59923-615-0159923-615-05- Official label
- DailyMed (National Library of Medicine), updated Oct 4, 2024
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