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Alembic Pharma receives final USFDA approval for Fenofibrate Tablets

Alembic Pharma receives final USFDA approval for Fenofibrate Tablets

Mumbai, Jan 23 (UNI) Pharma Major Alembic Pharma on Thursday said it has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Fenofibrate Tablets USP, 54 mg and 160 mg.

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD) Tricor Tablets, 54 mg and 160 mg, of AbbVie Inc.,company said in a filing with BSE.

Fenofibrate Tablets USP, 54 mg and 160 mg are indicated as an adjunct to diet to reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL-C in adult patients with primary hypercholesterolemia or mixed dyslipidaemia and for treatment of adult patients with severe hypertriglyceridemia.

Alembic has a cumulative total of 113 ANDA approvals (100 final approvals and 13 tentative approvals) from USFDA.

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