| NDC Code | 43063-489-14 |
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| Package Description | 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-489-14) |
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| Product NDC | 43063-489 |
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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 | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19920801 |
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| End Marketing Date | 20150430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074330 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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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] |
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