| NDC Code | 0591-2880-01 |
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| Package Description | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0591-2880-01) |
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| Product NDC | 0591-2880 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Verapamil Hydrochloride |
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| Non-Proprietary Name | Verapamil Hydrochloride |
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| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 19900529 |
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| End Marketing Date | 20260930 |
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| Marketing Category Name | NDA |
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| Application Number | NDA019614 |
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| Manufacturer | Teva Pharmaceuticals Inc |
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| Substance Name | VERAPAMIL HYDROCHLORIDE |
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| Strength | 120 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | 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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