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Aurobindo, Sun Pharma recall products in U.S. market


While Aurobindo Pharma is recalling Cyanocobalamin Injection, which is used to treat lack of vitamin B12, Sun Pharma is recalling a drug used to increase the production of tears in eyes

While Aurobindo Pharma is recalling Cyanocobalamin Injection, which is used to treat lack of vitamin B12, Sun Pharma is recalling a drug used to increase the production of tears in eyes

Leading drug firms Aurobindo Pharma, Sun Pharma and Jubilant are recalling different products in the U.S. market for various reasons, as per the latest enforcement report by the U.S. Food and Drug Administration (USFDA).

While Aurobindo Pharma is recalling Cyanocobalamin Injection, which is used to treat and prevent lack of vitamin B12, Mumbai-based Sun Pharma is recalling a drug used to increase the production of natural tears in eyes.

Similarly, Jubilant Cadista is recalling a drug which is used to treat different inflammatory conditions.

Jubilant Cadista Pharmaceuticals is a fully-owned subsidiary of Cadista Holdings Inc, which is a part of the Noida-based Jubilant Life Sciences.

The USFDA stated that Aurobindo Pharma USA Inc, a unit of Hyderabad-based drug major, is recalling 4,33,809 vials of Cyanocobalamin injection for being a “Subpotent Drug”.

The New Jersey-based firm initiated the recall on April 5.

The U.S. health regulator noted that U.S.-based Sun Pharmaceutical Industries Inc is recalling 73,030 boxes of Cequa (cyclosporine ophthalmic solution) for being a “Subpotent Drug”.

Besides, there was low out-of-specification results obtained for assay and the presence of particulate matter in the affected lot, USFDA stated as reasons for the company to initiate the recall.

The company, a subsidiary of Sun Pharma, initiated the recall on April 1, this year.

The USFDA noted that Salisbury-based Jubilant Cadista Pharmaceuticals Inc is recalling 19,222 bottles of Methylprednisolone tablets for being “Subpotent”.

As per the U.S. health regulator, New Jersey-based Macleods Pharma USA Inc is also recalling 4,872 bottles of a drug used to treat or prevent osteoporosis, manufactured at Baddi (Himachal Pradesh) due to “Failed content uniformity specifications.” The USFDA has classified the recalls as Class III, which is initiated in a “situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.”

The U.S. generic drug market was estimated to be around USD 115.2 billion in 2019. It is the largest market for pharmaceutical products.



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