The reason for the recall is "CGMP Deviation: Presence of dark brown
discoloration on edges of tablets," USFDA said. The ongoing voluntary
recall is a class II recall, the report said.
https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/jubilant-cadista-inc-recalls-63216-bottles-of-erosive-esophagitis-tablets/articleshow/71792552.cms
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