Jubilant Cadista recalls 5mg Prochlorperazine tablets due to subpotent drug levels. Affected lots may not contain enough active ingredient for effective treatment.
Subpotent Drug: Out of specification for assay at the 18-month stability timepoint.
Jubilant Cadista is recalling 5mg Prochlorperazine Maleate tablets that may have insufficient active ingredient. This could mean the medication isn't effective for treating conditions like nausea or vomiting.
The tablets failed quality testing at the 18-month stability point, meaning they may contain less active ingredient than labeled. This could lead to ineffective treatment if the medication isn't working as intended.
Prescription patients who received these specific tablets from Jubilant Cadista. Those with medical conditions requiring precise medication dosing may be most affected.
Check for the product name 'Prochlorperazine Maleate Tablets, USP 5mg, 100 tablets, RX Only'. Look for the lot number 21P0336 and expiration date 04/2023 on the packaging.
Verify the lot number and expiration date on the packaging to confirm if your tablets are affected.
The tablets failed quality testing at the 18-month stability point, meaning they may contain less active ingredient than labeled.
Check the lot number and expiration date on the packaging. If it matches lot 21P0336 with expiration 04/2023, contact your healthcare provider for guidance.
This is a low-risk recall as the tablets may not be effective, not a risk of serious injury or harm.
We’ve drafted a message you can send Jubilant Cadista to request your refund or repair — edit it as you like.
Subject: Recall D-0096-2023 — Jubilant Cadista Jubilant Cadista Hello, I own a Jubilant Cadista that is covered by recall D-0096-2023 from Jubilant Cadista. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
