| NDC Code | 52125-776-02 |
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| Package Description | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-776-02) |
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| Product NDC | 52125-776 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diltiazem Hydrochlorideextended Release |
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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 | 20131106 |
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| End Marketing Date | 20170826 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074984 |
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| Manufacturer | REMEDYREPACK INC. |
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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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