ABILIFY - 24236-839-35 - (ABILIFY)

Alphabetical Index


Drug Information of ABILIFY

Product NDC: 24236-839
Proprietary Name: ABILIFY
Non Proprietary Name: ABILIFY
Active Ingredient(s): 15    mg/1 & nbsp;   ABILIFY
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ABILIFY

Product NDC: 24236-839
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20101214

Package Information of ABILIFY

Package NDC: 24236-839-35
Package Description: 30 TABLET in 1 CANISTER (24236-839-35)

NDC Information of ABILIFY

NDC Code 24236-839-35
Proprietary Name ABILIFY
Package Description 30 TABLET in 1 CANISTER (24236-839-35)
Product NDC 24236-839
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ABILIFY
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101214
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ARIPIPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of ABILIFY


General Information