Granules Pharmaceuticals is recalling 20mg amphetamine capsules (NDC 70010-032-01) due to failed impurities and degradation specifications. This is a prescription product with a lot number of GPC250179A and expiration date 06-22-2027.
Failed Impurities/Degradation Specifications:
Granules Pharmaceuticals is recalling prescription amphetamine capsules (20mg, 100 capsules) because they failed impurities and degradation specifications. This means the product may contain harmful substances that could cause health risks if taken.
The capsules failed impurities and degradation specifications, meaning they may contain harmful substances that could cause health risks when taken. This is a prescription product that requires medical supervision.
Prescription users of the 20mg amphetamine capsules (NDC 70010-032-01) with lot number GPC250179A are affected. People who have taken these capsules since their manufacture date are at risk.
Check for the product name 'Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate', 20mg, 100 capsules, NDC 70010-032-01, lot number GPC250179A, and expiration date 06-22-2027.
Look for the NDC code 70010-032-01 and lot number GPC250179A on the product packaging.
The official recall notice states that the product failed impurities and degradation specifications, so it is not safe to use.
The recall record does not specify a remedy, so the official notice does not provide instructions on what to do with the product.
Check for the NDC code 70010-032-01 and lot number GPC250179A on the product packaging.
We’ve drafted a message you can send Granules Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0672-2025 — Granules Pharmaceuticals Granules Pharmaceuticals Hello, I own a Granules Pharmaceuticals that is covered by recall D-0672-2025 from Granules 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.
