NDC 60687-191 – Aripiprazole

Aripiprazole 15 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC60687-191

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205064
Marketed since
June 5, 2015
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (2)

Package NDCDescriptionSince
60687-191-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-191-21) / 1 TABLET in 1 BLISTER PACK (60687-191-11)Jun 5, 2015
60687-191-9420 BLISTER PACK in 1 CARTON (60687-191-94) / 1 TABLET in 1 BLISTER PACK (60687-191-11)Aug 1, 2025

Recalls mentioning this NDC

Other Aripiprazole products