| NDC Code | 53489-531-03 |
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| Package Description | 250 TABLET in 1 BOTTLE, PLASTIC (53489-531-03) |
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| Product NDC | 53489-531 |
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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 |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19930429 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA073582 |
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| Manufacturer | Mutual Pharmaceutical Company, 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],beta-Adrenergic Blocker [EPC],Thiazide-like Diuretic [EPC],Increased Diuresis [PE] |
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