Alembic Pharmaceuticals Limited recalls Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited
Alembic Pharmaceuticals recalls 20mg Telmisartan tablets due to label mixup. This medication is prescription-only and may be confused with other products. Consumers should contact the manufacturer for details.
Lower-risk recall
Labeling: Label-mixup
Contact the company & request your remedy
What happened, in plain English
Alembic Pharmaceuticals is recalling 20mg Telmisartan tablets that may have label mix-ups. This could lead to confusion with other medications, especially since the product is prescription-only. Read more at govinfonow.com/recall/36279-alembic-telmisartan-tablets-20mg-recall-label-mixup-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/36279-alembic-telmisartan-tablets-20mg-recall-label-mixup-hazard · Updated October 4, 2026 · FDA enforcement record: FDA #D-0326-2021
Cite this page
“Alembic Telmisartan Tablets 20mg Recall: Label Mixup Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36279-alembic-telmisartan-tablets-20mg-recall-label-mixup-hazard. Based on FDA recall #D-0326-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0326-2021%22&limit=1).
Why it’s dangerous
Label mix-ups can cause confusion between similar medications, potentially leading to incorrect dosing or use. Since this is a prescription-only drug, patients must be careful to follow their healthcare provider's instructions.
Who’s affected
Prescription patients who have the specific 20mg Telmisartan tablets with the NDC 62332-087-30 and lot number 1905005661 are affected. Those using the medication without proper labeling could be at risk of confusion.
How to tell if you have this one
Check for the NDC code 62332-087-30 and lot number 1905005661 on the packaging. The product is a 30-count bottle of Telmisartan tablets, 20mg strength, sold only with a prescription.
- Brand
Alembic Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Label
Look for the NDC code 62332-087-30 and lot number 1905005661 on the packaging.
Questions people ask
Is this product safe to use?
The recall is for potential label mix-ups, not safety issues. The product is safe if labeled correctly, but confusion with other medications is a risk.
How can I confirm if I have the recalled product?
Check for the NDC code 62332-087-30 and lot number 1905005661 on the packaging. The product is a 30-count bottle of Telmisartan tablets, 20mg strength, sold only with a prescription.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact Alembic Pharmaceuticals for further instructions.
Contact Alembic Pharmaceuticals
We’ve drafted a message you can send Alembic Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0326-2021 — Alembic Pharmaceuticals Alembic Pharmaceuticals Hello, I own a Alembic Pharmaceuticals that is covered by recall D-0326-2021 from Alembic Pharmaceuticals. 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-0326-2021 (March 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0326-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.