As per the information available on the USFDA website, Cipla is recalling the drug for "failed impurities and degradation specifications".
The vials were manufactured by Cipla at its Pithampur manufacturing facility, near Indore, for Princeton-based Dr Reddy's Laboratories Inc, it added.
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The recall of the drugs has been initiated under Class-III which FDA defined as "a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences".
A query sent to a company spokesperson remained unanswered.
Cipla, which has presence in over 150 countries, sells more than 2,000 products across various therapeutic categories.
The company has 34 manufacturing facilities that make active pharmaceutical ingredients (APIs) and formulations.
Cipla shares were trading at Rs 674.50 apiece on the BSE, down 1.97% from their previous close.
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