Dr. Reddy's Rugby antihistamine and nasal decongestant tablets with failed dissolution specifications are being recalled. This recall addresses potential safety concerns with the product's effectiveness.
Failed Dissolution Specifications
Dr. Reddy's Rugby antihistamine and nasal decongestant tablets (Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release) are being recalled due to failed dissolution specifications. This means the tablets may not release medication properly, potentially affecting treatment effectiveness.
The tablets failed to dissolve correctly as specified, which could lead to inconsistent medication release. This might result in the product not working as intended for treating allergies or cold symptoms.
People who purchased the Rugby antihistamine and nasal decongestant tablets with the specific NDC number 0536-1242-07 are affected. Those using the product for allergies or cold symptoms may be at risk of improper medication delivery.
Check for the NDC number 0536-1242-07 on the packaging. The product was distributed by Rugby Laboratories in Livonia, MI, and made in India with the lot number AC2106452F.
Look for the NDC number 0536-1242-07 on the packaging to confirm if the product is recalled.
The recall is due to failed dissolution specifications, which may affect the product's effectiveness but does not indicate immediate safety risks. The product is not considered dangerous for use.
The recall record does not specify a remedy, so there is no action required beyond checking the product details.
Check the NDC number 0536-1242-07 on the packaging. The product was distributed by Rugby Laboratories in Livonia, MI, and made in India with the lot number AC2106452F.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0379-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0379-2022 from Dr. Reddy's. 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.
