Dr Reddy's Labs, FDC recall generic medications in US over manufacturing issues
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-11-18 07:32 GMT | Update On 2024-11-18 07:32 GMT
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New Delhi: Dr Reddy's Laboratories and FDC Ltd, are recalling generic medications in the US over manufacturing defects. According to the US Food and Drug Administration (USFDA), the recalls were initiated after issues were identified with Timolol Maleate ophthalmic solution, and multiple strengths of Morphine Sulfate extended-release tablets respectively.
As per the latest Enforcement Report by Food and Drug Administration (USFDA), the US-based subsidiary of Dr Reddy's Laboratories is recalling multiple strengths of Morphine Sulfate extended-release tablets in the US.
The medication is used to relieve severe and persistent pain.
As per the USFDA, Princeton-based Dr Reddy's Laboratories Inc is recalling 2,040 bottles of 15 mg Morphine Sulfate extended-release tablets due to "Failed Impurities/Degradation Specification".
The drugmaker is also recalling another 532 100-count bottles of the medication in 30 mg strength for the same reason, USFDA stated.
Dr Reddy's initiated the Class II nationwide recall on October 22 this year.
Read also: Dr Reddy's Labs recalls over 3 lakh bottles of Cinacalcet tablets in US over manufacturing issues
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