| NDC Code | 61919-920-90 |
|---|
| Package Description | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-920-90) |
|---|
| Product NDC | 61919-920 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Non-Proprietary Name | Venlafaxine Hydrochloride |
|---|
| Dosage Form | CAPSULE, DELAYED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150101 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020699 |
|---|
| Manufacturer | DIRECT RX |
|---|
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
|---|
| Strength | 75 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
|---|