| NDC Code | 47335-882-44 |
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| Package Description | 10 CARTON in 1 CARTON (47335-882-44) > 1 AMPULE in 1 CARTON (47335-882-40) > 10 mL in 1 AMPULE |
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| Product NDC | 47335-882 |
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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 | 20210526 |
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| Marketing Category Name | NDA |
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| Application Number | NDA078405 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | NICARDIPINE HYDROCHLORIDE |
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| Strength | 2.5 |
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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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