ABILIFY - 21695-002-30 - (ARIPIPRAZOLE)

Alphabetical Index


Drug Information of ABILIFY

Product NDC: 21695-002
Proprietary Name: ABILIFY
Non Proprietary Name: ARIPIPRAZOLE
Active Ingredient(s): 5    mg/1 & nbsp;   ARIPIPRAZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ABILIFY

Product NDC: 21695-002
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021436
Marketing Category: NDA
Start Marketing Date: 20021115

Package Information of ABILIFY

Package NDC: 21695-002-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (21695-002-30)

NDC Information of ABILIFY

NDC Code 21695-002-30
Proprietary Name ABILIFY
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (21695-002-30)
Product NDC 21695-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ARIPIPRAZOLE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021115
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
Substance Name ARIPIPRAZOLE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of ABILIFY


General Information