| NDC Code | 66993-580-85 |
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| Package Description | 1 BOTTLE in 1 CARTON (66993-580-85) > 90 CAPSULE in 1 BOTTLE |
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| Product NDC | 66993-580 |
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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 | 20160701 |
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| End Marketing Date | 20210131 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022460 |
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| Manufacturer | Prasco Laboratories |
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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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