Sun Pharma, Glenmark recall products due to manufacturing issues in United States

Reportedly, the Mumbai-based drug major is recalling the affected lot due to “water leakage” leading to deviation from current good manufacturing practices (cGMP).

Sun Pharma, Glenmark recall products due to manufacturing issues in United States
The affected lot was produced at Sun Pharma's Halol (Gujarat) based manufacturing plant, as per PTI.

Sun Pharma and Glenmark are recalling products in the United States due to issues in the manufacturing process of the products. According to a report by the US Food and Drug Administration (USFDA), a US-based unit of Sun Pharma is recalling 50,680 vials of Testosterone Cypionate Injection, used to treat low testosterone in adult males, in the American market.

Reportedly, the Mumbai-based drug major is recalling the affected lot due to “water leakage” leading to deviation from current good manufacturing practices (cGMP). Meanwhile, the company is also recalling 27 vials of the same medication due to cGMP deviations, USFDA said as reported by news agency PTI.

“Manufacturing deviations were reported due to an abnormal appearance on parts of machinery,” it added. The affected lot was produced at Sun Pharma’s Halol (Gujarat) based manufacturing plant, as per PTI.

New Jersey-based Sun Pharmaceutical Industries Inc, a unit of the company, initiated the Class II nationwide (US) recall of the affected lots last month. 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.

Mumbai-headquartered Glenmark, on the other hand is recalling 98,307 packs of Mometasone Furoate Topical Solution, a medication used to treat skin conditions such as eczema, psoriasis, allergies, and rash. New Jersey-based Glenmark Pharmaceuticals Inc is recalling the lot, which rolled out from the company’s Baddi (Himachal Pradesh) plant, due to “Defective Container”, the USFDA stated.

The company initiated the nationwide recall, which the US health regulator classified as Class III, on June 16. 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 generic drug market was estimated to be around USD 115.2 billion in 2019. It is by far the largest market for pharmaceutical products in the world.

In the last financial year, India’s pharma exports stood at around USD 24.62 billion with the US, the UK, South Africa, Russia, and Nigeria emerging as the top five destinations.

(With inputs from PTI)

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