| NDC Code: |
41616-759 |
| Proprietary Name: |
Venlafaxine Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
Venlafaxine Hydrochloride |
| Dosage Form: |
TABLET, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
18-08-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA091272 |
| Labeler: |
SUN PHARMA GLOBAL INC. |
| Substance Name: |
VENLAFAXINE HYDROCHLORIDE |
| Active Numerator Strength: |
75 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |
|
