Azurity Pharmaceuticals recalls Zenzedi (Dextroamphetamine Sulfate) 30mg tablets due to potential label mix-up. This CII prescription drug, sold by Arbor Pharmaceuticals, requires immediate attention for safety.
Labeling: Label Mix-up
Azurity Pharmaceuticals is recalling Zenzedi (Dextroamphetamine Sulfate) 30mg tablets because of a potential label mix-up. This could lead to confusion about which medication a patient is taking, especially since it's a controlled substance (CII) that requires a prescription.
The recall is for a potential label mix-up, meaning the packaging might show the wrong medication name or dosage. This could cause confusion about which prescription drug a patient is taking, especially since Zenzedi is a controlled substance (CII) that requires a prescription and has specific usage instructions.
Prescription patients who have the specific Zenzedi 30mg tablets with NDC 24338-856-03 and lot number F230169A are affected. Those who take this medication for ADHD or other conditions are most at risk due to the controlled substance status.
Check for Zenzedi (Dextroamphetamine Sulfate) 30mg tablets with NDC 24338-856-03 and lot number F230169A. The product was manufactured for Arbor Pharmaceuticals and sold in the U.S. by prescription.
Verify the product label matches the specific NDC 24338-856-03 and lot number F230169A.
The recall is for a potential label mix-up, not a safety issue with the medication itself. However, confusion could lead to incorrect use, so it's recommended to check your medication.
The recall does not specify a remedy, so there is no action required beyond checking the label for the specific NDC and lot number.
No, Zenzedi is a prescription-only medication (CII) and requires a valid prescription from a healthcare provider.
We’ve drafted a message you can send Azurity to request your refund or repair — edit it as you like.
Subject: Recall D-0323-2024 — Azurity Azurity Hello, I own a Azurity that is covered by recall D-0323-2024 from Azurity. 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.
