| NDC Code | 58118-0734-0 |
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| Package Description | 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKET (58118-0734-0) |
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| Product NDC | 58118-0734 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoprolol Succinate |
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| Non-Proprietary Name | Metoprolol Succinate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20100722 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090615 |
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| Manufacturer | Clinical Solutions Wholesale |
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| Substance Name | METOPROLOL SUCCINATE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
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