| NDC Code | 59762-0152-1 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-0152-1) |
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| Product NDC | 59762-0152 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Trandolapril And Verapamil Hydrochloride |
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| Proprietary Name Suffix | Er |
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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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| End Marketing Date | 20180228 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020591 |
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| Manufacturer | Greenstone LLC |
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| Substance Name | TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE |
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| Strength | 1; 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 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA] |
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