NDC Code: |
59762-0182 |
Proprietary Name: |
Venlafaxine Hydrochloride |
Suffix: |
|
Non-Proprietary Name: |
VENLAFAXINE HYDROCHLORIDE |
Dosage Form: |
CAPSULE, EXTENDED RELEASE |
Method: |
ORAL |
Original Marketing Date: |
02-06-2011 |
Category Name: |
NDA AUTHORIZED GENERIC |
Application Number: |
NDA020699 |
Labeler: |
GREENSTONE LLC |
Substance Name: |
VENLAFAXINE HYDROCHLORIDE |
Active Numerator Strength: |
150 |
Active Ingredient Unit: |
mg/1 |
Pharm Classes: |
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
DEA Schedule: |
|