NDC 27241-051 – Aripiprazole

Aripiprazole 2 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC27241-051

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Ajanta Pharma USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206174
Marketed since
May 30, 2017
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
27241-051-0330 TABLET in 1 BOTTLE (27241-051-03)May 30, 2017
27241-051-08500 TABLET in 1 BOTTLE (27241-051-08)May 30, 2017

Recalls mentioning this NDC

Other Aripiprazole products