| NDC Code | 68462-329-10 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-329-10) |
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| Product NDC | 68462-329 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Trandolapril And Verapamil Hydrochloride |
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| Non-Proprietary Name | Trandolapril And Verapamil Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20150225 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079135 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE |
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| Strength | 4; 240 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA] |
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