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Lupin, Sun Pharma and Jubilant Cadista recall drugs in US market


Lupin, Sun Pharma and Jubilant Cadista recall drugs in US market
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
Leading generic drug makers Lupin, Sun Pharma and Jubilant Cadista are recalling different products in the US, the world’s largest market for medicines, for different reasons.
According to the latest enforcement report by the US Food and Drug Administration (USFDA), the US-based unit of Lupin is recalling 17,814 bottles of Cefprozil for Oral Suspension USP, a second-generation antibiotic used to treat infections of the ear, skin and other bacterial infections. ....

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Sun Pharma, Dr Reddy's, Aurobindo recall products in the U.S. market


Dr Reddy s Laboratories is recalling 2,24,710 (500 count) bottles of Atorvastatin Calcium tablets.
Leading home grown drug makers Sun Pharma, Dr Reddy s Laboratories, Aurobindo Pharma and Jubilant Pharma are recalling products in the U.S. market, the world s largest market for pharmaceutical products, for various reasons.
As per the latest Enforcement Report by the U.S. Food and Drug Administration (USFDA), Sun Pharma is recalling Cequa ophthalmic solution, which is used to treat chronic dry eye.
The U.S.-based subsidiary of the Mumbai-based drug major is recalling 37,400 cartons (60 vials per carton) of the ophthalmic solution for being subpotent , the U.S. health regulator said. ....

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Sun Pharma, Dr Reddy's, Aurobindo recall products in the US market


Leading home grown drug makers Sun Pharma, Dr Reddy s Laboratories, Aurobindo Pharma and Jubilant Pharma are recalling products in the US market, the world s largest market for pharmaceutical products, for various reasons.
As per the latest Enforcement Report by the US Food and Drug Administration (USFDA), Sun Pharma is recalling Cequa ophthalmic solution, which is used to treat chronic dry eye.
The US-based subsidiary of the Mumbai-based drug major is recalling 37,400 cartons (60 vials per carton) of the ophthalmic solution for being subpotent , the US health regulator said.
The Princeton (NJ) based firm initiated the nationwide recall of the affected lot on February 22, this year, it added. ....

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