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A Validated HPLC/MS Limit Test Method for a Potential Genotoxic Impurity in Cilostazol and its Quantification in the API and in the Commercially Available Drug Product
 
 
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Article Versions Notes

Sci. Pharm. 2016, 84(2), 289-303; https://doi.org/10.3797/scipharm.1507-04
Action Date Notes Link
article pdf uploaded. 7 September 2016 11:30 CEST Version of Record https://www.mdpi.com/2218-0532/84/2/289/pdf
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