Glenmark Pharmaceuticals recalls Indomethacin 25mg capsules that may be mislabeled as Naproxen. This labeling error could lead to incorrect medication use. Consumers should check product labels and contact the manufacturer for details.
Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen
Glenmark is recalling Indomethacin 25mg capsules that may be mislabeled as Naproxen. This mix-up could cause someone to take the wrong medication, which might lead to health issues.
The capsules may have incorrect labeling, showing Naproxen instead of Indomethacin. This mix-up could lead to taking the wrong medication, which might cause health problems if used incorrectly.
People who have the specific Indomethacin 25mg capsules with the listed lot numbers and expiration dates are affected. Those who take the medication as prescribed are most at risk if mislabeled.
Check the label for 'Indomethacin 25mg Capsules, USP, 100-count bottle, Rx Only'. Look for lot numbers 19231903, 19231858, 19231881, or 19233484/19233490 with expiration dates of 4/2025 or 8/2025.
Look for the label indicating 'Indomethacin 25mg Capsules, USP, 100-count bottle, Rx Only' on the bottle.
The capsules may be mislabeled as Naproxen instead of Indomethacin, which could lead to incorrect medication use.
Check the label for 'Indomethacin 25mg Capsules, USP, 100-count bottle, Rx Only' and look for lot numbers 19231903, 19231858, 19231881, or 19233484/19233490 with expiration dates of 4/2025 or 8/2025.
The recall does not specify a remedy, so contact Glenmark Pharmaceuticals for further instructions.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0123-2024 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0123-2024 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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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.