FDA Enforcement Report Details Ongoing Class III Recall of Dabigatran Etexilate Capsules
FDA enforcement records detail an ongoing recall of 2,717 cartons of Dabigatran etexilate Capsules distributed nationwide.
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FDA enforcement records detail an ongoing recall of 2,717 cartons of Dabigatran etexilate Capsules distributed nationwide.
Ascend Laboratories, LLC is recalling one lot of 75 mg Dabigatran Etexilate Capsules nationwide after a stability test failed impurity limits, according to the FDA enforcement record.
Ascend Laboratories, LLC is conducting a nationwide Class III recall of one lot of 75 mg dabigatran etexilate capsules due to failed impurity specifications, according to FDA records.
An official FDA report lists an ongoing nationwide Class III recall for one lot of prescription medication.
An FDA enforcement report lists an ongoing nationwide recall of one lot of amlodipine and olmesartan medoxomil tablets distributed by Ascend Laboratories over failed dissolution specifications.