NDC 67877-430 – Aripiprazole

Aripiprazole 2 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC67877-430

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207105
Marketed since
February 27, 2019
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (5)

Package NDCDescriptionSince
67877-430-01100 TABLET in 1 BOTTLE (67877-430-01)Feb 27, 2019
67877-430-0330 TABLET in 1 BOTTLE (67877-430-03)Feb 27, 2019
67877-430-05500 TABLET in 1 BOTTLE (67877-430-05)Feb 27, 2019
67877-430-321 BLISTER PACK in 1 CARTON (67877-430-32) / 7 TABLET in 1 BLISTER PACKFeb 27, 2019
67877-430-3810 BLISTER PACK in 1 CARTON (67877-430-38) / 10 TABLET in 1 BLISTER PACK (67877-430-33)Feb 27, 2019

Recalls mentioning this NDC

Other Aripiprazole products