NDC 14335-132
Sodium Nitroprusside 0.2 mg per 1 mL injection, solution
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 and packages it | Problems found, fixed voluntarilyJun 30, 2023 · 4 inspections |
Product details
- Generic drug
- Nitroprusside: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.2 mg per 1 mL
- Approval
- ANDA ANDA215846
- On the market since
- Dec 31, 2022
- Package NDCs
14335-132-01- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2022
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