| NDC Code | 68071-3214-3 |
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| Package Description | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3214-3) |
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| Product NDC | 68071-3214 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diltiazem Hydrochloride |
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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, COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20151001 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074984 |
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| Manufacturer | NuCare Pharmaceutical, Inc. |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 240 |
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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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