NDC 65162-898 – Aripiprazole

Aripiprazole 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC65162-898

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204838
Marketed since
June 20, 2016
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (4)

Package NDCDescriptionSince
65162-898-0330 TABLET in 1 BOTTLE (65162-898-03)Jun 20, 2016
65162-898-0990 TABLET in 1 BOTTLE (65162-898-09)Jun 20, 2016
65162-898-111000 TABLET in 1 BOTTLE (65162-898-11)Jun 20, 2016
65162-898-50500 TABLET in 1 BOTTLE (65162-898-50)Jun 20, 2016

Recalls mentioning this NDC

Other Aripiprazole products