Preferred Pharmaceuticals recalls 0.5mg alprazolam tabs (NDCs 68788-7595-3, 68788-7595-6, 68788-7595-9) due to potential cross contamination from Breckenridge Pharmaceuticals. Rx only medication.
CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Preferred Pharmaceuticals is recalling 0.5mg alprazolam tabs that were manufactured by Breckenridge Pharmaceuticals due to potential cross contamination. This recall affects specific bottle counts and expiration dates. The medication is prescription-only and should be checked for the correct NDC numbers.
The recall is due to potential cross contamination from Breckenridge Pharmaceuticals during manufacturing. This could lead to unintended medication mix-ups, but the exact risk level is not specified in the notice.
Prescription holders of the 0.5mg alprazolam tabs with NDCs 68788-7595-3, 68788-7595-6, or 68788-7595-9. Those with the specific lot numbers and expiration dates listed are most at risk.
Check your alprazolam tabs for the NDC numbers: 68788-7595-3 (30-count), 68788-7595-6 (60-count), or 68788-7595-9 (90-count). Also look for the specific lot numbers and expiration dates listed in the recall notice.
Identify your alprazolam tabs by checking the NDC numbers and lot numbers listed in the recall notice.
The recall is due to potential cross contamination from Breckenridge Pharmaceuticals during manufacturing.
The affected products are 0.5mg alprazolam tabs with NDCs 68788-7595-3 (30-count), 68788-7595-6 (60-count), and 68788-7595-9 (90-count).
Check the NDC numbers on your product: 68788-7595-3, 68788-7595-6, or 68788-7595-9. Also verify the lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0505-2023 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0505-2023 from Preferred 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.
