Aripiprazole (Page 15 of 15)

Package/Label Display Panel

Aripiprazole Tablets, USP

2 mg

500 Tablets

Bottle Label
(click image for full-size original)
ARIPIPRAZOLE aripiprazole tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0904-6656(NDC:13668-217)
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
MICROCRYSTALLINE CELLULOSE
CROSPOVIDONE (15 MPA.S AT 5%)
Hydroxypropyl Cellulose (1600000 WAMW)
MAGNESIUM STEARATE
MANNITOL
SILICON DIOXIDE
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape ROUND Size 5mm
Flavor Imprint Code 5;17
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0904-6656-40 500 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA201519 04/28/2015
Labeler — Major Pharmaceuticals (191427277)

Revised: 05/2022 Major Pharmaceuticals

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

https://medlibrary.org/lib/rx/meds/aripiprazole-51/page/15/

Clinical Trials

MedLibrary.org

Medication Sections

RSS Feeds

About

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2022. All Rights Reserved.