Aripiprazole

Product NDC
46708-254
11-digit product format
467080254
Labeler code
46708
Product ID
46708-254_5108607e-5633-4b19-82f9-6c48720960c4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
Alembic Pharmaceuticals Limited
Application
ANDA202101
Marketing category
ANDA
Marketing start
2015-04-28
Substance
ARIPIPRAZOLE
Active strength
2 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
82VFR53I78ARIPIPRAZOLE129722-12-9ARIPIPRAZOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
46708-254-1046708025410100 TABLET in 1 CARTON (46708-254-10) 100 tablet2015-04-28NoNoHistorical
46708-254-304670802543030 TABLET in 1 BOTTLE (46708-254-30) 30 tablet2015-04-28NoNoHistorical
46708-254-3146708025431100 TABLET in 1 BOTTLE (46708-254-31) 100 tablet2015-04-28NoNoHistorical
46708-254-4546708025445180 TABLET in 1 BOTTLE (46708-254-45) 180 tablet2015-04-28NoNoHistorical
46708-254-604670802546060 TABLET in 1 BOTTLE (46708-254-60) 60 tablet2015-04-28NoNoHistorical
46708-254-7146708025471500 TABLET in 1 BOTTLE (46708-254-71) 500 tablet2015-04-28NoNoHistorical
46708-254-91467080254911000 TABLET in 1 BOTTLE (46708-254-91) 1000 tablet2015-04-28NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AripiprazoleAlembic Pharmaceuticals Limited2023-01-27Human Prescription Drug Label3