Aripiprazole

Product NDC
50090-7564
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203908
Marketing category
ANDA
Substance
ARIPIPRAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7564-030 TABLET in 1 BOTTLE (50090-7564-0) 2025-05-28NoHistorical
50090-7564-190 TABLET in 1 BOTTLE (50090-7564-1) 2025-05-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AripiprazoleA-S Medication Solutions2025-06-03Human Prescription Drug Label2