| NDC Code | 51285-047-02 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (51285-047-02) |
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| Product NDC | 51285-047 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ziac |
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| Non-Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19931026 |
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| End Marketing Date | 20250531 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020186 |
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| Manufacturer | Teva Women's Health LLC |
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| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
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| Strength | 2.5; 6.25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |
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