Aripiprazole (Page 11 of 11)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 2 mg (30 Tablets Bottle)

NDC 71205-480-30
Aripiprazole
Tablets USP
2 mg
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
Rx only 30 Tablets

71205-480-30
(click image for full-size original)

ARIPIPRAZOLE aripiprazole tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71205-480(NDC:65862-661)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 2 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
FD&C BLUE NO. 2
FERRIC OXIDE YELLOW
Product Characteristics
Color GREEN Score no score
Shape RECTANGLE Size 8mm
Flavor Imprint Code 61;H
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71205-480-30 30 TABLET in 1 BOTTLE None
2 NDC:71205-480-60 60 TABLET in 1 BOTTLE None
3 NDC:71205-480-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203908 10/08/2015
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (71205-480), RELABEL (71205-480)

Revised: 10/2020 Proficient Rx LP

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