Aripiprazole

Product NDC
68071-3906
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA205064
Marketing category
ANDA
Substance
ARIPIPRAZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3906-414 TABLET in 1 BOTTLE (68071-3906-4) 2025-10-16NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AripiprazoleNuCare Pharmaceuticals, Inc.2025-10-16HUMAN PRESCRIPTION DRUG LABEL1