Lupin Pharmaceuticals recalls 150mg Rifampin Capsules (30-count) due to subpotent drug and failed impurities. Rx-only product with specific batch numbers. Contact for return instructions.
Subpotent Drug and Failed Impurities/Degradation Specifications
Lup: Lupin Pharmaceuticals is recalling 150mg Rifampin Capsules (30-count bottles) because they may not contain the correct amount of active ingredient and have failed quality tests. This could lead to ineffective treatment if used as prescribed.
The capsules may not contain the full dose of rifampin due to subpotent drug issues. Failed impurities and degradation specifications mean the product might not work as intended for treating infections.
Prescription patients who have received this specific bottle of Rifampin Capsules. Those with medical conditions requiring precise dosing are at higher risk.
Check for the 30-count bottle labeled 'Rifampin Capsules USP 150mg', Rx Only. Look for batch numbers A200816 (exp 1/2024) or A201248 (exp 3/2024) on the packaging.
Verify the bottle has 30 capsules labeled 'Rifampin Capsules USP 150mg, Rx Only' with batch numbers A200816 or A201248.
The recall states the product may not contain the correct amount of active ingredient and has failed quality tests, so it is not safe to use as intended.
Check for the 30-count bottle with 'Rifampin Capsules USP 150mg, Rx Only' and batch numbers A200816 (exp 1/2024) or A201248 (exp 3/2024).
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for instructions on returning the product.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0283-2024 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0283-2024 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.
