NDC Code(s) : 62135-531-30
Packager : Chartwell RX, LLC

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

venlafaxine hydrochloridevenlafaxine hydrochloride TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62135-531
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VENLAFAXINE HYDROCHLORIDE(UNII: 7D7RX5A8MO)
(VENLAFAXINE - UNII:GRZ5RCB1QG) 		VENLAFAXINE225 mg
Inactive Ingredients
Ingredient Name Strength
DIBASIC CALCIUM PHOSPHATE DIHYDRATE(UNII: O7TSZ97GEP)
HYPROMELLOSE, UNSPECIFIED(UNII: 3NXW29V3WO)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)(UNII: XRK36F13ZZ)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
MAGNESIUM STEARATE(UNII: 70097M6I30)
POLYVINYL ACETATE(UNII: 32K497ZK2U)
TALC(UNII: 7SEV7J4R1U)
POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW)(UNII: 23ZQ42JZZH)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
TRIETHYL CITRATE(UNII: 8Z96QXD6UM)
STEARETH-20(UNII: L0Q8IK9E08)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
CARNAUBA WAX(UNII: R12CBM0EIZ)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
WATER(UNII: 059QF0KO0R)
Product Characteristics
Color white (white to off white, imprinted in blue) Score no score
Shape ROUND Size 13 mm
Flavor Imprint Code 225mg
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:62135-531-3030 in 1 BOTTLE Type 0: Not a Combination Product29/03/2023
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA209193 12/26/2019

LABELER - Chartwell RX, LLC(079394054)

PRINCIPAL DISPLAY PANEL

Venlafaxine Hydrochloride Extended Release Tablets 225 mg- NDC 62135-531-30 -30s Bottle Label

Venlafaxine Hydrochloride ER Tablets