MFDA orders recall of batch of Antidep tablets

2 days ago

Maldives Food and Drug Authority (MFDA) has ordered the recall of a batch of Antidep 25 mg tablets. In a statement Sunday, MFDA said that clinical investigations uncovered active ingredients in batch no. 2141H003 of Antidep 25 mg tablets were lower than they should be. Generic name: Imipramine hydrochloride Brand, dosage form, strength: (Antidep 25 mg) film coated tablet Manufacturer/ country of origin: Torrent