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Shenzhen Nexconn Pharmatechs Ltd
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active pharmaceutical ingredient
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dabigatran etexilate mesylate
Specification: 99%+ purity, unknown single impurity<0.1%
Detail: Dabigatran etexilate mesylate was first approved by EMA on May 18,2008, then approved by the USA FDA on Oct 19,2010, and approved by P*** on Jan 21,2011. It was developed and marketed as Pradaxa by Boehringer Ingelheim in DE a...
2
rivaroxaban
Specification: 99%+ purity, unknown single impurity<0.1%
Detail: Rivaroxaban was first approved by Health Canada on September 15, 2008, then approved by European Medicine Agency£¨EMA£©on September 30, 2008, and approved by the US Food and Drug Administration£¨FDA£© on July 01,2011. It was d...
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