Prescription Drug Information: Venlafaxine Hydrochloride (Page 12 of 12)

PRINCIPAL DISPLAY PANEL

DRUG: Venlafaxine Hydrochloride

GENERIC: Venlafaxine Hydrochloride

DOSAGE: CAPSULE, EXTENDED RELEASE

ADMINSTRATION: ORAL

NDC: 70518-2532-0

COLOR: gray

SHAPE: CAPSULE

SCORE: No score

SIZE: 16 mm

IMPRINT: E;73

PACKAGING: 30 in 1 BLISTER PACK

ACTIVE INGREDIENT(S):

  • VENLAFAXINE HYDROCHLORIDE 37.5mg in 1

INACTIVE INGREDIENT(S):

  • ETHYLCELLULOSE (20 MPA.S)
  • TITANIUM DIOXIDE
  • GELATIN, UNSPECIFIED
  • FERROSOFERRIC OXIDE
  • SODIUM LAURYL SULFATE
  • FERRIC OXIDE RED
  • HYPROMELLOSE 2910 (5 MPA.S)
  • SHELLAC
  • SUCROSE
  • STARCH, CORN
  • TALC
Remedy_Label
(click image for full-size original)
VENLAFAXINE HYDROCHLORIDE venlafaxine hydrochloride capsule, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70518-2532(NDC:65862-527)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 37.5 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
TALC
FERRIC OXIDE RED
GELATIN, UNSPECIFIED
TITANIUM DIOXIDE
SODIUM LAURYL SULFATE
FERROSOFERRIC OXIDE
SHELLAC
ETHYLCELLULOSE (20 MPA.S)
HYPROMELLOSE 2910 (5 MPA.S)
SUCROSE
Product Characteristics
Color gray (Opaque Grey) , orange (Opaque Peach) Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code E;73
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70518-2532-0 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA200834 01/08/2020
Labeler — REMEDYREPACK INC. (829572556)

Revised: 01/2020 REMEDYREPACK INC.

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