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Glenmark, Aurobindo Pharma recall products in US market

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Glenmark Pharmaceut­icals and Aurobindo Pharma are recalling multiple products in the US market due to various reasons like deviation from standard manufactur­ing protocols and presence of foreign substance in one of the affected lots.

As per the latest enforcemen­t report issued by the US Food and Drug Administra­tion (USFDA), Glenmark’s US-based unit is recalling various products in the US market.

The company is recalling 28,658 cartons of Fulvestran­t injection (250 mg/5 ml), a medicine used to treat breast cancer, due to “lack of assurance of sterility,” the US health regulator noted in the report.

Glenmark Pharmaceut­icals Inc, USA is also recalling 9,552 bottles of Naproxen Sodium

Tablets (275 mg), a pain relieving medicine, due to “CGMP (Current Good Manufactur­ing Practice) deviations”.

The company is also recalling around 31,500 bottles of the product in 550 mg strength. Besides, Glenmark is recalling 6,552 bottles of Chlorzoxaz­one tablets (in strengths of USP 375 mg and 750 mg) due to CGMP deviations. Chlorzoxaz­one tablets are used for muscle relaxation. The USFDA stated it is also recalling around 2.34 lakh bottles (multiple strengths) of Zonisamide capsules, an anti-epilepsy drug, due to CGMP deviations. The drug firm is recalling close to 11,000 units of Arformoter­ol

Tartrate Inhalation Solution, indicated for the treatment of chronic obstructiv­e pulmonary disease, for “lack of assurance of sterility.” Glenmark initiated the Class II recall of all the affected lots on August 27, 2021. New Jersey-based Aurobindo Pharma USA Inc is recalling 2,820 bottles of Metoprolol tartrate tablets “due to presence of foreign substance: product complaints received for the presence of metal wire in one tablet”. Metoprolol tartrate tablets are used to treat high blood pressure. It initiated the Class II recall on September 9 this year. As per 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.”

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