aripiprazole

Product NDC
63629-7003
11-digit product format
636297003
Labeler code
63629
Product ID
63629-7003_19629960-f7d5-434b-869d-6784b2a65c74
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA201519
Marketing category
ANDA
Marketing start
2015-04-28
Substance
ARIPIPRAZOLE
Active strength
10 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
63629-7003-16362970030130 TABLET in 1 BOTTLE (63629-7003-1) 30 tablet2016-05-16NoNoHistorical
63629-7003-26362970030260 TABLET in 1 BOTTLE (63629-7003-2) 60 tablet2024-10-29NoNoHistorical
63629-7003-36362970030328 TABLET in 1 BOTTLE (63629-7003-3) 28 tablet2024-10-29NoNoHistorical
63629-7003-46362970030490 TABLET in 1 BOTTLE (63629-7003-4) 90 tablet2017-12-26NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
aripiprazoleBryant Ranch Prepack2024-10-29HUMAN PRESCRIPTION DRUG LABEL105