Sun Phar­ma is­sues re­call for more than 34,000 bot­tles of blood pres­sure med­ica­tion

A blood pres­sure med­ica­tion pro­duced by gener­ics gi­ant Sun Phar­ma­ceu­ti­cals is be­ing re­called.

Sun Phar­ma is vol­un­tar­i­ly re­call­ing dil­ti­azem hy­drochlo­ride in a 360 mg dosage form across the US, ac­cord­ing to an en­force­ment re­port from the FDA. The drug is used to treat high blood pres­sure and angi­na.

The FDA’s re­port said the re­call stems from a “failed im­pu­ri­ty spec­i­fi­ca­tion” dur­ing test­ing as well as an­oth­er failed test at an FDA lab­o­ra­to­ry. The re­port said that the re­called prod­uct was pro­duced by Sun Phar­ma’s fa­cil­i­ty in Halol, In­dia, a city in the na­tion’s south­west state of Gu­jarat. The re­call it­self was is­sued on Jan. 13 of this year.

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