Lupin Pharmaceuticals recalls 30-count Rifampin Capsules USP 30: subpotent drug and failed impurities may not work as intended. Contact for return instructions.
Subpotent Drug and Failed Impurities/Degradation Specifications
Lupin Pharmaceuticals is recalling 30-count Rifampin Capsules USP 300mg bottles that may not contain the correct drug strength or have impurities. This could lead to treatment failure if used for medical purposes.
The capsules may have incorrect drug strength (subpotent) or impurities that could affect treatment effectiveness. This means the medication might not work as intended for medical conditions.
Prescription patients using Rifampin Capsules USP 300mg, 30-count bottles. Those with medical conditions requiring this medication are most at risk.
Check for the product name 'Rifampin Capsules USP 300mg', 30-count bottle, Rx Only. The NDC code is 68180-659-06 with expiration 1/2024.
Verify the product name, count, and expiration date on the bottle.
The capsules may have incorrect drug strength or impurities that could affect treatment effectiveness.
Check for Rifampin Capsules USP 300mg, 30-count bottle, Rx Only with NDC 68180-659-06 and expiration 1/2024.
The recall record does not specify a remedy or action steps.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0284-2024 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0284-2024 from Lupin 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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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.
