| NDC Code | 50436-6915-1 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50436-6915-1) |
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| Product NDC | 50436-6915 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Verapamil |
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| Non-Proprietary Name | 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 | 20121119 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200878 |
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| Manufacturer | Unit Dose Services |
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| Substance Name | VERAPAMIL 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],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA] |
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