Unichem Pharmaceuticals recalls 500-count busPIRone Hydrochloride Tablets (5mg) due to subpotent drug content. This may result in ineffective treatment for patients requiring precise dosing. No remedy specified in official notice.
Subpotent drug
Unichem Pharmaceuticals is recalling 500-count busPIRone Hydrochloride Tablets (5mg) because they may not contain enough active ingredient to be effective. This could lead to improper treatment outcomes for patients using the medication as prescribed.
The tablets contain subpotent drug content, meaning they have less active ingredient than intended. This could result in the medication being less effective than prescribed, potentially leading to inadequate treatment for patients who require precise dosing.
Patients prescribed busPIRone Hydrochloride Tablets (5mg) by a healthcare provider are affected. Those using the medication for specific medical conditions where precise dosing is critical may be at higher risk.
Look for busPIRone Hydrochloride Tablets (5mg) in 500-count bottles with NDC 29300-244-05. The product was manufactured by Unichem Laboratories LTD. in India and distributed by Unichem Pharmaceuticals USA Inc. in the US.
Verify if your medication matches the description: 500-count busPIRone Hydrochloride Tablets (5mg) with NDC 29300-244-05.
The recall is due to subpotent drug content, which may make the medication less effective. It is not safe to use as intended without confirmation of proper potency.
The official recall notice does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the medication.
The recall is for ineffective medication, not a physical hazard. There is no risk of serious injury from this product.
We’ve drafted a message you can send Unichem Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0511-2026 — Unichem Pharmaceuticals Unichem Pharmaceuticals Hello, I own a Unichem Pharmaceuticals that is covered by recall D-0511-2026 from Unichem 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.
