NDC Code(s) : 58118-3780-9, 58118-3780-3, 58118-3780-8, 58118-3780-0
Packager : Clinical Solutions Wholesale

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Venlafaxine Hydrochloridevenlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:58118-3780(NDC:60505-3780)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VENLAFAXINE HYDROCHLORIDE(UNII: 7D7RX5A8MO)
(VENLAFAXINE - UNII:GRZ5RCB1QG) 		VENLAFAXINE150 mg
Inactive Ingredients
Ingredient Name Strength
POWDERED CELLULOSE(UNII: SMD1X3XO9M)
GELATIN(UNII: 2G86QN327L)
FERRIC OXIDE RED(UNII: 1K09F3G675)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
HYPROMELLOSES(UNII: 3NXW29V3WO)
HYPROMELLOSE 2910 (6 MPA.S)(UNII: 0WZ8WG20P6)
ETHYLCELLULOSE (100 MPA.S)(UNII: 47MLB0F1MV)
Product Characteristics
Color orange (DARK ORANGE) Score no score
Shape CAPSULE (CAPSULE) Size 22 mm
Flavor Imprint Code EffexorXR;150
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:58118-3780-990 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product08/07/2013
2NDC:58118-3780-330 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product08/07/2013
3NDC:58118-3780-830 in 1 BLISTER PACK Type 0: Not a Combination Product08/07/2013
4NDC:58118-3780-01 in 1 PACKET Type 0: Not a Combination Product08/07/2013
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA authorized generic NDA020699 06/10/2011 06/21/2017

PRINCIPAL DISPLAY PANEL

venlafaxine-hydrochloride-150mgvenlafaxine-hydrochloride-150mgvenlafaxine-hydrochloride-150mgvenlafaxine-hydrochloride-150mg