Aripiprazole

Product NDC
71335-0667
11-digit product format
713350667
Labeler code
71335
Product ID
71335-0667_1971f9b7-ccbf-4b94-9cc9-1ad74cbd871e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aripiprazole
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA204838
Marketing category
ANDA
Marketing start
2016-06-20
Marketing end
0000-00-00
Substance
ARIPIPRAZOLE
Active strength
2 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
82VFR53I78ARIPIPRAZOLE129722-12-9ARIPIPRAZOLE