| NDC Code | 68071-1923-3 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-1923-3) |
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| Product NDC | 68071-1923 |
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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 | 20100415 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077298 |
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| Manufacturer | NuCare Pharmaceuticals, Inc. |
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| Substance Name | METOPROLOL SUCCINATE |
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| Strength | 100 |
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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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