| NDC Code | 43353-889-19 |
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| Package Description | 3060 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43353-889-19) |
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| Product NDC | 43353-889 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diltiazem Hydrochloride |
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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 | 20090925 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020401 |
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| Manufacturer | Aphena Pharma Solutions - Tennessee, LLC |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 180 |
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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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