| NDC Code | 70934-717-30 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (70934-717-30) |
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| Product NDC | 70934-717 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lisinopril And Hydrochlorothiazide |
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| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20200519 |
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| End Marketing Date | 20241130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077912 |
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| Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
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| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
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| Strength | 12.5; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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