| NDC Code | 68084-052-30 |
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| Package Description | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68084-052-30) |
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| Product NDC | 68084-052 |
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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 | 20130326 |
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| End Marketing Date | 20171231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074984 |
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| Manufacturer | American Health Packaging |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 120 |
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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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