| NDC Code | 70069-875-10 |
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| Package Description | 10 POUCH in 1 CASE (70069-875-10) / 1 BAG in 1 POUCH (70069-875-01) / 200 mL in 1 BAG |
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| Product NDC | 70069-875 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nicardipine Hydrochloride |
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| Non-Proprietary Name | Nicardipine Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20260420 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA220243 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | NICARDIPINE HYDROCHLORIDE |
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| Strength | .1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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