| NDC Code | 51655-029-52 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-029-52) |
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| Product NDC | 51655-029 |
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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 | 20150209 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077614 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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| Substance Name | CARVEDILOL |
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| Strength | 6.25 |
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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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