| NDC Code: |
65580-301 |
| Proprietary Name: |
venlafaxine hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
venlafaxine hydrochloride |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
30-09-2008 |
| Category Name: |
NDA |
| Application Number: |
NDA022104 |
| Labeler: |
UPSTATE PHARMA, LLC |
| Substance Name: |
VENLAFAXINE HYDROCHLORIDE |
| Active Numerator Strength: |
37.5 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |
|
