Ascend Laboratories recalls 10mg Aripiprazole tablets (NDC 67877-432-03) due to superpotent drug hazard. Rx-only product manufactured in India, distributed in the US. Check your prescription label for recall details.
Superpotent drug
Ascend Laboratories is recalling 10mg Aripiprazole tablets (30-count bottles) because they contain a superpotent drug that poses a risk. This is a prescription-only product distributed in the US that could be dangerous if misused or taken without proper medical supervision.
The product contains a superpotent drug that could cause serious health effects if not used as directed by a healthcare provider. This risk is particularly concerning for individuals who may not be properly monitored by their doctor.
Prescription holders who have the 10mg Aripiprazole tablets (30-count bottles) with NDC 67877-432-03. Patients under medical supervision are most at risk due to the drug's potency.
Look for 10mg Aripiprazole tablets in 30-count bottles with NDC code 67877-432-03. The product is prescription-only and manufactured in India by Alken Laboratories Ltd.
Verify if your prescription label matches the recalled product: 10mg Aripiprazole tablets, 30-count bottles, NDC 67877-432-03.
The official recall states it contains a superpotent drug, but no specific safety details are provided. Consult your healthcare provider for guidance.
Check your prescription label for 10mg Aripiprazole tablets in 30-count bottles with NDC 67877-432-03.
The recall does not specify a remedy, so contact your healthcare provider for advice on next steps.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0645-2025 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0645-2025 from Ascend Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
