Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Sumatriptan Succinate Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to Failed Impurities/Degradation Specifications; out-of-specification results obtained for related...

Date: December 26, 2019
Company: Sun Pharmaceutical Industries, 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 Sun Pharmaceutical Industries, Inc. directly.

Affected Products

Sumatriptan Succinate Tablets, 50 mg, packaged in a) 9 (1x9) Unit-of use blister card (NDC 62756-521-69) and b) 100 count bottles, (NDC 62756-521-88), Rx only, Sun Pharma, Cranbury, NJ

Quantity: 384/100 count bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.

Where Was This Sold?

Product was distributed throughout the United States to 96 distributors and 1 repacker/relabeler.

About Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc. has 40 total recalls tracked by RecallDetector.

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