NDC Code | 68071-4876-3 |
Package Description | 30 TABLET in 1 BOTTLE (68071-4876-3) |
Product NDC | 68071-4876 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Venlafaxine |
Non-Proprietary Name | Venlafaxine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100407 |
Marketing Category Name | ANDA |
Application Number | ANDA090555 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | VENLAFAXINE HYDROCHLORIDE |
Strength | 75 |
Strength Unit | mg/1 |
Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |