| NDC Code | 70954-390-10 |
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| Package Description | 100 TABLET in 1 BOTTLE (70954-390-10) |
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| Product NDC | 70954-390 |
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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 | 20211025 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215560 |
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| Manufacturer | ANI 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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