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Comparative Study|Journal Article|Research Support, Non-U.S. Gov't|Validation Study |
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276 |
| issn |
0731-7085 |
| pageRange |
271-276 |
| publicationName |
Journal of Pharmaceutical and Biomedical Analysis |
| startingPage |
271 |
| bibliographicCitation |
Kahsay G, Van Schepdael A, Adams E. Development and validation of a liquid chromatographic method for purity control of clopidogrel–acetylsalicylic acid in combined oral dosage forms. Journal of Pharmaceutical and Biomedical Analysis. 2012 Mar;61():271–6. doi: 10.1016/j.jpba.2011.12.019. |
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2012-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1016/j.jpba.2011.12.019
https://pubmed.ncbi.nlm.nih.gov/22226416 |
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https://portal.issn.org/resource/ISSN/0731-7085 |
| language |
English |
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https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Development and validation of a liquid chromatographic method for purity control of clopidogrel–acetylsalicylic acid in combined oral dosage forms |
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