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Volumn 47, Issue 3, 2008, Pages 553-559

Identification of a degradation product in stressed tablets of olmesartan medoxomil by the complementary use of HPLC hyphenated techniques

Author keywords

Degradation product; HPLC hyphenated technique; LC MS; LC NMR; Olmesartan medoxomil; Solvent elimination LC IR

Indexed keywords

CARBONYL DERIVATIVE; DIMER; DRUG; DRUG DEGRADATION PRODUCT; ESTER; OLMESARTAN;

EID: 43949099637     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2008.02.021     Document Type: Article
Times cited : (57)

References (24)
  • 1
    • 43949137328 scopus 로고    scopus 로고
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q1A(R2): Stability Testing of New Drug Substances and Products, Step 4, February 6, 2003. Available at: http://www.ich.org/.
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q1A(R2): Stability Testing of New Drug Substances and Products, Step 4, February 6, 2003. Available at: http://www.ich.org/.
  • 2
    • 43949104890 scopus 로고    scopus 로고
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q3A(R2): Impurities in New Drug Substances, Step 4, October 25, 2006. Available at: http://www.ich.org/.
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q3A(R2): Impurities in New Drug Substances, Step 4, October 25, 2006. Available at: http://www.ich.org/.
  • 3
    • 43949127814 scopus 로고    scopus 로고
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q3B(R2): Impurities in New Drug Products, Step 4, June 2, 2006. Available at: http://www.ich.org/.
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), ICH Harmonised Tripartite Guideline Q3B(R2): Impurities in New Drug Products, Step 4, June 2, 2006. Available at: http://www.ich.org/.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.