ABILIFY - 24236-991-19 - (ARIPIPRAZOLE)

Alphabetical Index


Drug Information of ABILIFY

Product NDC: 24236-991
Proprietary Name: ABILIFY
Non Proprietary Name: ARIPIPRAZOLE
Active Ingredient(s): 20    mg/1 & nbsp;   ARIPIPRAZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ABILIFY

Product NDC: 24236-991
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021436
Marketing Category: NDA
Start Marketing Date: 20130409

Package Information of ABILIFY

Package NDC: 24236-991-19
Package Description: 90 TABLET in 1 CANISTER (24236-991-19)

NDC Information of ABILIFY

NDC Code 24236-991-19
Proprietary Name ABILIFY
Package Description 90 TABLET in 1 CANISTER (24236-991-19)
Product NDC 24236-991
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ARIPIPRAZOLE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130409
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name ARIPIPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of ABILIFY


General Information