| NDC Code | 51655-389-52 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-389-52) |
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| Product NDC | 51655-389 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Valsartan And Hydrochlorothiazide |
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| Non-Proprietary Name | Valsartan And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20230329 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078020 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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| Substance Name | HYDROCHLOROTHIAZIDE; VALSARTAN |
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| Strength | 12.5; 160 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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