Sodium Nitroprusside 71288-0202
Product NDC
71288-0202- Manufacturer
- Meitheal Pharmaceuticals Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 6, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211016
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Nitroprusside | 50 mg/2mL |
Drug Class
Vasodilation [PE]Vasodilator [EPC]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02) / 2 mL in 1 VIAL, SINGLE-DOSE