Class II

Drug Recall: Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03

Ascend Laboratories, LLC · August 28, 2025

Reason for Recall

Superpotent drug

Distribution

Nationwide in the USA.

States Affected

NATIONWIDE

Quantity Affected

2,256 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0645-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.