| NDC Code | 0409-4350-03 |
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| Package Description | 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-4350-03) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0409-4350-13) |
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| Product NDC | 0409-4350 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diltiazem Hydrochloride |
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| Non-Proprietary Name | Diltiazem Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20050430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075853 |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC] |
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