| NDC Code | 0131-3267-46 |
|---|
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0131-3267-46) |
|---|
| Product NDC | 0131-3267 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100429 |
|---|
| End Marketing Date | 20180331 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA022104 |
|---|
| Manufacturer | UCB, Inc. |
|---|
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
|---|
| Strength | 150 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
|---|