| NDC Code | 70954-652-20 |
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| Package Description | 90 CAPSULE in 1 BOTTLE (70954-652-20) |
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| Product NDC | 70954-652 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Finasteride And Tadalafil |
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| Non-Proprietary Name | Finasteride And Tadalafil |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20250324 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA218499 |
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| Manufacturer | ANI Pharmaceuticals, Inc. |
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| Substance Name | FINASTERIDE; TADALAFIL |
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| Strength | 5; 5 |
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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], Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA] |
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