Endo Recalls Clonazepam ODT Due to Carton Label Displaying Incorrect Strength. Diana Ernst, RPh
On J, Endo announced a consumer level recall of one lot of clonazepam 0.25 mg. ODT which may also appear as clonazepam 0.125 mg ODT.
Drug Recall . DATE OF RECALL: J . DRUG NAME: Clonazepam ODT Tablets. RECALLING FIRM: Endo. REASON FOR RECALL: Endo announced a consumer level recall of one lot of clonazepam orally disintegrating 0.25 mg tablets because they may have been packaged in a carton labelled as 0.125 mg . FDA LINK:
On J, Endo USA, Inc. recalled Clonazepam 0.125mg and 0.25mg Orally Disintegrating tablets (ODT) from a single lot due to a packaging error.
recalled Clonazepam 0.125mg and 0.25mg Orally Disintegrating tablets (ODT) from a single lot due to a packaging error. Some cartons labeled as
J - Endo announced a consumer level recall of one lot of clonazepam 0.25 mg ODT which may also appear as clonazepam 0.125 mg ODT. The recall is expanded to include the 0.125 mg strength. The recall was first announced on J.
On J, Endo USA, Inc. voluntarily recalled a single lot of Clonazepam 0.125 mg and 0.25 mg Orally Disintegrating tablets (ODT)
ataxia, and confusion. Endo Recalls Clonazepam ODT Due to Carton Label Displaying Incorrect Strength. From empr.com 9:18 PM . 43.
recalled Clonazepam 0.125mg and 0.25mg Orally Disintegrating tablets (ODT) from a single lot due to a packaging error. Some cartons labeled
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