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Monday, June 4, 2018

Amphastar gets FDA OK to produce heparin in China unit


Amphastar announced that the U.S.FDA granted approval of the company’s abbreviated new drug application supplement for the manufacture of semi-purified heparin at the company’s subsidiary, Amphastar Nanjing Pharmaceuticals and the manufacture of heparin sodium USP at the company’s subsidiary, International Medication Systems, Limited.

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