Sun Pharma gets warning letter from USFDA over Halol unit

New Delhi: Drug major Sun Pharmaceutical Industries on Saturday said it has received a warning letter from the USFDA over violation of manufacturing norms in its facility at Halol in Gujarat.

The warning letter follows inspection of the facility in September 2014 by US Food and Drug Administration (USFDA) inspectors.

"Post the September 2014 inspection, the USFDA has withheld future product approvals from the Halol facility.

This situation may continue until all issues are resolved.

"Sun Pharma expects to request a re-inspection by USFDA upon completion of its remediation commitments," the company said in a statement.

The firm and the Halol facility will continue to supply important drug products to meet its obligations towards the customers and the patients who use its drugs in the US and around the world, it added.

"Sun Pharma will respond to this Warning Letter with a detailed plan within the stipulated timeframe," it said.

Commenting on the development, Sun Pharma Managing Director Dilip Shanghvi said, "While our team is working hard to ensure that the commitments made to the USFDA in September 2014 are fully completed, we will continue to cooperate with the USFDA and undertake any additional steps necessary to ensure that the US agency is completely satisfied with our remediation of the Halol facility."

He added: "We are pledged to being cGMP compliant and are committed to continuing to supply our customers and patients across the world with quality products that meet all specifications."

Sun Pharma said it had responded to the USFDA inspection observations with a "robust remediation process that is still ongoing, with significant investments in automation and training to enhance its Quality Systems".

The company has been working with external consultants to ensure its remediation activities have been completed in an appropriate manner, it added.

It further said since the inspection in September 2014, the company has communicated regularly with the USFDA on the progress of its remediation and on issues of product supply.