aripiprazole

Product NDC
63629-6999
11-digit product format
636296999
Labeler code
63629
Product ID
63629-6999_b33d1f1c-a8f2-4275-a060-e2226eb2a7e4
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
Marketing end
0000-00-00
Substance
ARIPIPRAZOLE
Active strength
5 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-6999-1EA - Each63629-69990f08589e-6608-4bc8-827a-dcfdd660a73d12017-06-15

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-6999-16362969990130 TABLET in 1 BOTTLE (63629-6999-1) 30 tablet2016-05-090000-00-00NoNoCurrent
63629-6999-26362969990228 TABLET in 1 BOTTLE (63629-6999-2) 28 tablet2016-05-090000-00-00NoNoCurrent
63629-6999-36362969990390 TABLET in 1 BOTTLE (63629-6999-3) 90 tablet2016-05-090000-00-00NoNoCurrent
63629-6999-46362969990460 TABLET in 1 BOTTLE (63629-6999-4) 60 tablet2022-02-080000-00-00NoNoCurrent
63629-6999-563629699905120 TABLET in 1 BOTTLE (63629-6999-5) 120 tablet2022-02-080000-00-00NoNoCurrent
63629-6999-66362969990615 TABLET in 1 BOTTLE (63629-6999-6) 15 tablet2019-03-070000-00-00NoNoCurrent