FDADecember 26, 2019drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

sun pharmaceuticalsun

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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