Lupin gets US regulator approval for cholesterol drug


Mumbai, Oct 22 (IANS): Pharma major Lupin Tuesday announced it has received final approval for marketing additional strengths of cholesterol-lowering drug Antara capsules in the American market.

The company has received final approval for its supplemental New Drug Application (sNDA) for Antara (Fenofibrate) capsules in 30 mg and 90 mg strengths from the US Food and Drug Administration (USFDA).

"The approval demonstrates Lupin's commitment to building its brand franchise in the US," said Vinita Gupta, chief executive officer.

Lupin Pharmaceuticals Inc., the company's US subsidiary, would commence marketing the product shortly, the company said in a statement.

LPI currently markets Antara capsules in strengths of 43 mg and 130 mg in the US market.

The new drug would be manufactured by Lupin.

Antara capsules are prescribed for treatment of high blood cholesterol, mixed dyslipidemia and high triglycerides in combination with diet.

As per the IMS MAT June 2013 data, the market in the US for fenofibrate is valued close to $1.5 billion.

  

Top Stories


Leave a Comment

Title: Lupin gets US regulator approval for cholesterol drug



You have 2000 characters left.

Disclaimer:

Please write your correct name and email address. Kindly do not post any personal, abusive, defamatory, infringing, obscene, indecent, discriminatory or unlawful or similar comments. Daijiworld.com will not be responsible for any defamatory message posted under this article.

Please note that sending false messages to insult, defame, intimidate, mislead or deceive people or to intentionally cause public disorder is punishable under law. It is obligatory on Daijiworld to provide the IP address and other details of senders of such comments, to the authority concerned upon request.

Hence, sending offensive comments using daijiworld will be purely at your own risk, and in no way will Daijiworld.com be held responsible.