| NDC Code | 68382-640-16 |
|---|
| Package Description | 90 CAPSULE in 1 BOTTLE (68382-640-16) |
|---|
| Product NDC | 68382-640 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dutasteride And Tamsulosin Hydrochloride |
|---|
| Non-Proprietary Name | Dutasteride And Tamsulosin Hydrochloride |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180604 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207769 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE |
|---|
| Strength | .5; .4 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA], Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC] |
|---|