Cipla Limited (BSE: 500087) (NSE: CIPLA EQ), an India-based pharmaceutical company, has received final approval from the United States Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Icatibant Injectable 30mg/3mL, it was reported on Tuesday.
The product is indicated for the treatment of acute hereditary angioedema attacks in adults 18 years of age and older.
Icatibant Injectable 30mg/3mL is an AP-rated generic version of Shire's Firazyr.
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