| NDC Code | 70934-211-90 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-211-90) |
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| Product NDC | 70934-211 |
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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 | 20181227 |
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| End Marketing Date | 20230731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077614 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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| Substance Name | CARVEDILOL |
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| Strength | 12.5 |
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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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