Glenmark Pharmaceuticals Inc., USA recalls Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark
Glenmark recalls specific batches of Telmisartan and Hydrochlorothiazide tablets due to difficult blister opening and tablet breaks. Affected lots have expiration dates through August 2023.
Lower-risk recall
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Contact the company & request your remedy
What happened, in plain English
Glenmark is recalling certain batches of Telmisartan and Hydrochlorothiazide tablets because the blister packs are hard to open and tablets break during opening. This could lead to improper medication use if the tablets are not taken correctly. Read more at govinfonow.com/recall/34488-glenmark-telmisartan-hydrochlorothiazide-tablets-recall-blister-difficulty-opening.
Source Summary by GovInfoNow · govinfonow.com/recall/34488-glenmark-telmisartan-hydrochlorothiazide-tablets-recall-blister-difficulty-opening · Updated September 23, 2026 · FDA enforcement record: FDA #D-1305-2022
Cite this page
“Glenmark Telmisartan/Hydrochlorothiazide Tablets Recall: Blister Difficulty Opening.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/34488-glenmark-telmisartan-hydrochlorothiazide-tablets-recall-blister-difficulty-opening. Based on FDA recall #D-1305-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1305-2022%22&limit=1).
Why it’s dangerous
The blister packs are difficult to open, causing tablets to break. This may lead to improper medication use if the tablets are not taken correctly.
Who’s affected
People with prescriptions for these specific tablet batches. Those who have the affected lots (with expiration dates through August 2023) are most at risk.
How to tell if you have this one
Check for the product name 'Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only'. Look for specific lot numbers: 17210935, 17210936, 17211206, 17211652, 17211655, or 17211658 with expiration dates through August 2023.
- Brand
Glenmark- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
nationwide- NDC
68462-840-13, 68462-841-13, 68462-842-13
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1305-2022 | Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot no 2, Phase-2, Pharma Zone, SEZ Pithampur, District Dhar, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc, USA, Mahwah, NJ 07430, NDC 68462-842-13.; Lots 17210935 & 17210936., Exp Date 05/2023 Lot 17211206, Exp Date 06/2023 Lots 17211652, 17211655 & 17211658, Exp Date 08/2023 | 72288 units |
| D-1306-2022 | Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot no 2, Phase-2, Pharma Zone, SEZ Pithampur, District Dhar, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc,m USA, Mahwah, NJ 07430, NDC 68462-841-13.; Lots 17210929 & 17210930, Exp Date 05/2023; Lot 17211203, Exp Date 06/2023 & Lots 17211643, 17211646 & 17211649, Exp Date 08/2023 | — |
What to do — step by step
Check Product Details
Identify the lot number and expiration date on the packaging to determine if it is affected.
Questions people ask
Why is this product being recalled?
The recall is due to complaints of difficult blister opening and tablet breaks during opening.
What should I do if I have the affected product?
The official notice does not specify a remedy for this recall.
Which lots are affected?
Lots 17210935, 17210936, 17211206, 17211652, 17211655, and 17211658 with expiration dates through August 2023.
Contact Glenmark
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-1305-2022 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-1305-2022 from Glenmark. 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-1305-2022 (June 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1305-2022 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.