| NDC Code | 62756-369-83 |
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| Package Description | 30 TABLET in 1 BOTTLE (62756-369-83) |
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| Product NDC | 62756-369 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
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| Non-Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20220401 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090654 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
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| Strength | 50; 100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |
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