NEW DELHI: Drug firm Lupin’s US arm, Lupin Pharmaceuticals Inc, is recalling 12,480 bottles of Paroxetine extended-release tablets on account of failed dissolution specifications from the US market.

freispiele online Zeewolde Lupin Pharmaceuticals Inc is recalling 12,480 bottles of Paroxetine extended-release tablets in the strength of 12.5 mg manufactured by Lupin Ltd at its Pithampur plant in Madhya Pradesh, the USFDA said in its latest Enforcement Report.

what is the human dose of ivermectin The reason for the recall is “failed dissolution specifications: out of specification observed in dissolution testing at 3 month long term stability study”, the report added.

Wichita slots online kostenlose spiele spielen The product is used for treatment of depression, panic disorder and social anxiety disorder.

site gay sans virus immitigably As per the United States Food and Drug Administration (USFDA), the ongoing voluntary nationwide in the USA recall is a class III recall.

single klubb i sjøholt Patzún According to the USFDA, a class III recall is initiated in a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.