Pro Pharma's new drug, antatory hydrochloride, gets FDA approval
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Last Update: 2020-06-08
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Source: Internet
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Author: User
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recently, Plo Pharmaceuticals announced that its wholly-owned sub-
company
(http://Zhejiang Jutai Pharmaceutical Co., Ltdto the United States
FDAto declare thenew drughttp:// (http://application (andA), that is, the U.Simitationpharmaceutical(http://application) has been approvedon hydrochloric acid amphetamine reprieve syltoss
hydrochloric acid amphetamine reprieve sylline is suitable for the treatment of severe depression and seasonal affective disorder The Drug (http:// developed by VALEANT INTERNATIo nAL BARBADOS SR and launched in the United States on August 28, 2003 the main manufacturers of amphetamine-release tablets in the United States are PAR, TEVA, etc., and there is currently no product spree of the dosage form (http:// marketed The antatone hydrochloric acid reprieve was developed by Plo Pharmaceuticals in cooperation with Tulex Pharmaceutical Co Ltd., Inc of the United States, and to date, Plo Pharmaceuticals has invested approximately $1.5 million in research and development on the amphetamine reprieve project The antatone hydrochloride release tablet is the first generic drug approved by the FDA, and this time it has obtained FDA approval, marking prodruge's eligibility for sale in the U.S market
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