| NDC Code | 70771-1356-9 |
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| Package Description | 90 CAPSULE in 1 BOTTLE (70771-1356-9) |
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| Product NDC | 70771-1356 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dutasteride And Tamsulosin Hydrochloride |
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| Non-Proprietary Name | Dutasteride And Tamsulosin Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20180604 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207769 |
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| Manufacturer | Zydus Lifesciences Limited |
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| Substance Name | DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE |
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| Strength | .5; .4 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA], Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
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