| NDC Code | 10135-733-01 |
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| Package Description | 100 TABLET in 1 BOTTLE (10135-733-01) |
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| Product NDC | 10135-733 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atenolol And Chlorthalidone |
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| Non-Proprietary Name | Atenolol And Chlorthalidone Tablet |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20220301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215560 |
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| Manufacturer | MARLEX PHARMACEUTICALS, INC |
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| Substance Name | ATENOLOL; CHLORTHALIDONE |
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| Strength | 50; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC] |
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