Aripiprazole

Product NDC
50090-4863
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA207105
Marketing category
ANDA
Substance
ARIPIPRAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-4863-030 TABLET in 1 BOTTLE (50090-4863-0) 2020-01-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AripiprazoleA-S Medication Solutions2024-10-16Human Prescription Drug Label5