ARIPIPRAZOLE (Page 13 of 13)

Principal Display Package

NDC: 70934-662-30

label
(click image for full-size original)
ARIPIPRAZOLE aripiprazole tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70934-662(NDC:16729-279)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 5 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
HYDROXYPROPYL CELLULOSE (TYPE L)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
FD&C BLUE NO. 2
Product Characteristics
Color blue Score no score
Shape RECTANGLE (modified rectangle) Size 8mm
Flavor Imprint Code A5
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70934-662-30 30 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA206251 04/07/2020
Labeler — Denton Pharma, Inc. dba Northwind Pharmaceuticals (080355546)
Registrant — Denton Pharma, Inc. dba Northwind Pharmaceuticals (080355546)
Establishment
Name Address ID/FEI Operations
Denton Pharma, Inc. dba Northwind Pharmaceuticals 080355546 repack (70934-662)

Revised: 08/2021 Denton Pharma, Inc. dba Northwind Pharmaceuticals

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