| NDC Code | 43353-798-17 |
|---|
| Package Description | 6030 TABLET in 1 BOTTLE, PLASTIC (43353-798-17) |
|---|
| Product NDC | 43353-798 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120507 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079098 |
|---|
| Manufacturer | Aphena Pharma Solutions - Tennessee, LLC |
|---|
| 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] |
|---|