| NDC Code | 70518-2213-0 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2213-0) |
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| Product NDC | 70518-2213 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
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| Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20190714 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205391 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
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| Strength | 20; 12.5 |
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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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