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United States Food and Drug Administration (US FDA)
US FDA issues EIR for Lupin’s injectable facility in Nagpur
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Venus Remedies’ VRP-034 receives QIDP designation from US FDA
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Lupin receives US FDA Establishment Inspection Report for Somerset facility
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Sanofi India receives marketing authorisation for Rezurock in India
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BWXT medical submits drug master file for Actinium-225 API to U.S. FDA
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Zydus Cadila gets US FDA nod to market generic tension headache tablets
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