Sodium Nitroprusside In 0.9% Sodium Chloride 70436-0207
Product NDC
70436-0207- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 31, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA215846
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Nitroprusside | .5 mg/mL |
Drug Class
Vasodilation [PE]Vasodilator [EPC]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 CARTON (70436-207-80) / 100 mL in 1 VIAL, SINGLE-DOSE