Aripiprazole

Product NDC
72189-456
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
Direct_Rx
Application
ANDA205064
Marketing category
ANDA
Substance
ARIPIPRAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-456-3030 TABLET in 1 BOTTLE (72189-456-30) 2023-03-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AripiprazoleDirect_Rx2025-01-22HUMAN PRESCRIPTION DRUG LABEL2