| NDC Code | 70436-205-80 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (70436-205-80) / 50 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 70436-205 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Nitroprusside In 0.9% Sodium Chloride |
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| Non-Proprietary Name | Sodium Nitroprusside In 0.9% Sodium Chloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20221231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215846 |
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| Manufacturer | Slate Run Pharmaceuticals, LLC |
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| Substance Name | SODIUM NITROPRUSSIDE |
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| Strength | .2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Vasodilation [PE], Vasodilator [EPC] |
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