NDC 71205-938
Terbutaline Sulfate 2.5 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 24979-132.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant | Taoyuan City, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
| Apace Packaging LLC | Fountain Run, KY, United States | Packages it | No problems foundJan 13, 2022 · 6 inspections |
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Packages it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Terbutaline: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA211832
- On the market since
- Jul 13, 2020
- Package NDCs
71205-938-0071205-938-3071205-938-5571205-938-6071205-938-90- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2022
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