| NDC Code | 0456-2615-00 |
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| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0456-2615-00) |
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| Product NDC | 0456-2615 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tiazac |
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| Proprietary Name Suffix | Extended Release |
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| Non-Proprietary Name | Diltiazem Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20101225 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020401 |
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| Manufacturer | Forest Laboratories, Inc. |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 300 |
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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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