| NDC Code | 50742-250-10 |
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| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50742-250-10) |
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| Product NDC | 50742-250 |
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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 | 20190614 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208783 |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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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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