Aurobindo Pharma, Sun Pharma recall Rasagiline Tablets, Cequa from US market

The US health regulator stated that Aurobindo Pharma is recalling 9,890 bottles of Rasagiline Tablets, a medication indicated for the treatment of Parkinson's disease, from the US.

Published On 2023-10-09 07:00 GMT   |   Update On 2023-10-09 07:00 GMT

New Delhi: Leading drug makers Sun Pharmaceutical Industries and Aurobindo Pharma are recalling products from the US market due to manufacturing issues, according to the US Food & Drug Administration.As per the latest Enforcement Report issued by the American health regulator, a US-based subsidiary of Mumbai-based Sun Pharma is recalling 69,707 cartons of Cequa (cyclosporine...

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New Delhi: Leading drug makers Sun Pharmaceutical Industries and Aurobindo Pharma are recalling products from the US market due to manufacturing issues, according to the US Food & Drug Administration.

As per the latest Enforcement Report issued by the American health regulator, a US-based subsidiary of Mumbai-based Sun Pharma is recalling 69,707 cartons of Cequa (cyclosporine ophthalmic solution) from the US market.

The medication is used for the treatment of dry eyes.

New Jersey-based Sun Pharmaceutical Industries Inc is recalling the product for being "Subpotent'', USFDA stated.

The company initiated the nationwide (US) Class III recall on September 7 this year.

As per the USFDA, a Class III recall is initiated in a "situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences".

The US health regulator stated that Aurobindo Pharma is recalling 9,890 bottles of Rasagiline Tablets, a medication indicated for the treatment of Parkinson's disease, from the US.

New Jersey-based Aurobindo Pharma USA Inc, a unit of the Hyderabad-based drug major, is recalling the affected lot due to "Failed dissolution specifications", the USFDA noted.

Read also: 3 baby formula makers get USFDA warning letter to correct manufacturing process controls

The company initiated the Class II recall in the US on August 2 this year.

As per the USFDA, a class II recall is initiated in a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Read also: Popular antacid Digene gel receives warning alert from DCGI, Abbott initiates recall

The Indian pharmaceutical industry is the third largest in the world by volume with a current market size of around USD 50 billion.

India exported pharmaceuticals worth Rs 1,75,040 crore in 2021-22, including bulk drugs/drug intermediates.

Read also: USFDA accepts Sun Pharma NDA for alopecia areata drug Deuruxolitinib

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Article Source : PTI

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