Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Temozolomide Capsules Recalled by Amerigen Pharmaceuticals Inc. Due to Failed Dissolution Specifications

Date: December 20, 2018
Company: Amerigen Pharmaceuticals Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Amerigen Pharmaceuticals Inc. directly.

Affected Products

Temozolomide Capsules, 180 mg, packaged in a 14 count bottles, Rx only, Mfd, by: Stason Pharmaceuticals, Inc., Irvine, CA, Dist. By: Amerigen Pharmaceuticals, Lyndhurst, NJ ---- NDC 43975-256-14

Quantity: 771 bottles

Why Was This Recalled?

Failed Dissolution Specifications

Where Was This Sold?

Product was distributed to 4 wholesalers and 2 retail accounts who may have further distributed the products.

About Amerigen Pharmaceuticals Inc.

Amerigen Pharmaceuticals Inc. has 4 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report