Last Updated on October 15, 2024 by The Health Master
Zydus Lifesciences has received final approval from the US Food and Drug Administration (USFDA) to market Colestipol Hydrochloride tablets in the strength of 1mg.
The company said in a statement that the tablets are indicated as adjunctive therapy to diet for the reduction of elevated serum total and LDL-C in patients with primary hypercholesterolemia (elevated LDL-C) who do not respond adequately to diet.
Colestipol Hydrochloride is a highly complex macro molecule drug substance with little or no systemic absorption, it said.
It also said that Zydus’ ANDA is only the second generic application approved by USFDA for this product. The drug will be manufactured at the group’s formulation manufacturing facility at SEZ, Ahmedabad.
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