| NDC Code | 63739-016-10 |
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| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-016-10) / 10 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 63739-016 |
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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 | McKesson Corporation dba SKY Packaging |
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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], Cytochrome P450 3A4 Inhibitors [MoA] |
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