Prescription Drug Information: Venlafaxine Hydrochloride (Page 11 of 11)

Package/Label Display Panel

NDC: 42708-054-30

Label
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VENLAFAXINE HYDROCHLORIDE venlafaxine hydrochloride capsule, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42708-054(NDC:0093-7385)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 75 mg
Inactive Ingredients
Ingredient Name Strength
FERROSOFERRIC OXIDE
DIBUTYL SEBACATE
ETHYLCELLULOSE (7 MPA.S)
GELATIN, UNSPECIFIED
POLYETHYLENE GLYCOL 400
POVIDONE K30
PROPYLENE GLYCOL
SHELLAC
SUCROSE
STARCH, CORN
FD&C YELLOW NO. 6
TALC
TITANIUM DIOXIDE
D&C YELLOW NO. 10
POTASSIUM HYDROXIDE
Product Characteristics
Color brown (buff) Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code 93;7385;93;7385
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:42708-054-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076565 07/01/2010
Labeler — QPharma Inc (030620888)
Registrant — Teva Pharmaceuticals USA, Inc. (001627975)
Establishment
Name Address ID/FEI Operations
Northwind Pharmaceuticals, LLC 036986393 repack (42708-054)

Revised: 01/2023 QPharma Inc

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