Jubilant Cadista Pharmaceuticals, Inc. recalls Meclizine hydrochloride tablets USP, 12.5 mg, 100 count HDPE bottle, Rx only, Manufactured by: Jubilant Cadista
Jubilant Cadista recalls 12.5mg Meclizine tablets sold without FDA approval due to premature release. Consumers should check NDC 59746-122-06 and lot #17P0430 for affected products.
Recall notice
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Contact the company & request your remedy
What happened, in plain English
Jubilant Cadista is recalling 12.5 mg Meclizine hydrochloride tablets that were released before FDA approval. This means the product may not be safe for use as it wasn't properly tested. Read more at govinfonow.com/recall/41116-jubilant-cadista-meclizine-tablets-recalled-unapproved-drug-release.
Source Summary by GovInfoNow · govinfonow.com/recall/41116-jubilant-cadista-meclizine-tablets-recalled-unapproved-drug-release · Updated October 7, 2026 · FDA enforcement record: FDA #D-0082-2018
Cite this page
“Jubilant Cadista Meclizine Tablets Recalled: Unapproved Drug Release.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41116-jubilant-cadista-meclizine-tablets-recalled-unapproved-drug-release. Based on FDA recall #D-0082-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0082-2018%22&limit=1).
Why it’s dangerous
The tablets were released to the market before receiving final FDA approval. This means the product may not have undergone proper safety testing, potentially posing health risks.
Who’s affected
People who have purchased the 12.5 mg Meclizine tablets with NDC 59746-122-06 and lot number 17P0430 are affected. Those using prescription medications should be cautious as the product was released without FDA approval.
How to tell if you have this one
Check for the NDC code 59746-122-06 and lot number 17P0430 on the bottle. The product is a prescription-only 12.5 mg Meclizine hydrochloride tablet in a 100-count HDPE bottle.
- Brand
Jubilant Cadista- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 59746-122-06 and lot number 17P0430 on the bottle to confirm if it's affected.
Questions people ask
Why is this product being recalled?
The product was released to the market before receiving final FDA approval, which means it may not have undergone proper safety testing.
How can I check if I have the recalled product?
Check for the NDC code 59746-122-06 and lot number 17P0430 on the bottle.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact the manufacturer for guidance.
Contact Jubilant Cadista
We’ve drafted a message you can send Jubilant Cadista to request your refund or repair — edit it as you like.
Subject: Recall D-0082-2018 — Jubilant Cadista Jubilant Cadista Hello, I own a Jubilant Cadista that is covered by recall D-0082-2018 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.
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Where this comes from
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.
- Official source: FDA Recall #D-0082-2018 (October 30, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0082-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.