| NDC Code | 68071-2633-8 |
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| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2633-8) |
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| Product NDC | 68071-2633 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Carvedilol |
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| Non-Proprietary Name | Carvedilol |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20161001 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078384 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | CARVEDILOL |
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| Strength | 3.125 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC] |
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