Aripiprazole

Product NDC
46708-255
11-digit product format
467080255
Labeler code
46708
Product ID
46708-255_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
5 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
46708-255-1046708025510100 TABLET in 1 CARTON (46708-255-10) 100 tablet2015-04-28NoNoHistorical
46708-255-304670802553030 TABLET in 1 BOTTLE (46708-255-30) 30 tablet2015-04-28NoNoHistorical
46708-255-3146708025531100 TABLET in 1 BOTTLE (46708-255-31) 100 tablet2015-04-28NoNoHistorical
46708-255-4546708025545180 TABLET in 1 BOTTLE (46708-255-45) 180 tablet2015-04-28NoNoHistorical
46708-255-604670802556060 TABLET in 1 BOTTLE (46708-255-60) 60 tablet2015-04-28NoNoHistorical
46708-255-7146708025571500 TABLET in 1 BOTTLE (46708-255-71) 500 tablet2015-04-28NoNoHistorical
46708-255-91467080255911000 TABLET in 1 BOTTLE (46708-255-91) 1000 tablet2015-04-28NoNoHistorical

Related DailyMed Labels

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