Ranbaxy Lab suffers another setback as US FDA bans its 4th plant, shares slump 20%

Comments 0
FDA prohibits Ranbaxy Lab from distributing in the US the drugs manufactured using active pharmaceutical ingredients in Toansa facility in Punjab. FDA prohibits Ranbaxy Lab from distributing in the US the drugs manufactured using active pharmaceutical ingredients in Toansa facility in Punjab.
SummaryRanbaxy prohibited from producing drugs for American market from its Toansa facility in Punjab.

In yet another setback for

Ranbaxy Laboratories Ltd, the US health regulator banned the import of products from its fourth plant, halting the shipment of all the company's drugs to the US from India.

Citing manufacturing norm violations, the US Food and Drug Administration (USFDA) prohibited Ranbaxy Laboratories from distributing drugs produced at the Toansa unit in Punjab, including medicines made by the company's Ohm Laboratories facility in New Jersey.

In an order yesterday, the USFDA also prohibited Ranbaxy from providing active pharmaceutical ingredients from Toansa to other companies, including other Ranbaxy facilities, that make products for American consumers.

"We are taking swift action to prevent substandard quality products from reaching US consumers," said Carol Bennett, acting director of the Office of Compliance in the FDA's Center for Drug Evaluation and Research.

The USFDA said it exercised its authority under a provision in a January 2012 consent decree, which permits the agency to extend those terms to any Ranbaxy-owned or operated facility if an FDA inspection finds it in violation of the Federal Food, Drug, and Cosmetic Act or FDA regulations, including current good manufacturing practice requirements.

"This development is clearly unacceptable and an appropriate management action will be taken upon completion of the internal investigation," Ranbaxy Chief Executive Officer and Managing Director Arun Sawhney said.

Expressing disappointment, the company said it "would like to apologise to all its stakeholders for the inconvenience caused by the suspension."

Japanese parent Daiichi Sankyo confirmed the Toansa plant is now subject to certain terms of the consent decree of permanent injunction entered against Ranbaxy in January 2012.

Ranbaxy will cooperate with the USFDA and comply with the consent decree in both letter and spirit, it said.

Ranbaxy Lab shares plunged 19.54 per cent to Rs 335.65 at the close on the BSE.

"With this import alert, the operations of the company in US business, which contributes around 40 per cent, could come under impact unless it can compensate for the same at the earliest and manage a smooth supply of key raw material," said Sarabjit Kour Nangra, Angel Broking VP - Research Pharma.

According to Arvind Bothra, Vice President of Institutional Research at Religare Capital Markets, Ranbaxy's US quarterly sales of USD 125 million (base) may be hit by 35-40 per cent for the next three to four quarters, until they get site transfers for key products.

"The US and India

Single Page Format
Ads by Google

More from Health

Reader´s Comments
| Post a Comment
Please Wait while comments are loading...