NDC 10271-101
Terbutaline Sulfate 1 mg per 1 mL injection
On the label: United Biomedical Inc., Asia.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| United Biomedical Inc., Asia | Location not on file | Makes it | Not inspected on record |
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
- Dec 15, 2014
- Package NDCs
10271-101-10- Official label
- DailyMed (National Library of Medicine), updated Sep 26, 2014
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