NDC 14335-171
Dobutamine 12.5 mg per 1 mL injection, solution, concentrate
On the label: Hainan Poly Pharm. Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hainan Poly Pharm. Co., Ltd. | Haikou, China | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 30, 2023 · 4 inspections |
Product details
- Generic drug
- Dobutamine: every company that makes it
- Form
- injection, solution, concentrate
- Strength
- 12.5 mg per 1 mL
- Approval
- ANDA ANDA216131
- On the market since
- Jun 1, 2021
- Package NDCs
14335-171-01- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2023
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