Development and validation of a stability indicating HPLC method for determination of lisinopril, lisinopril degradation product and parabens in the lisinopril extemporaneous formulation

Journal of Pharmaceutical and Biomedical Analysis

Volumn 37, Issue 3, 2005, Pages 559-567

  Beasley, Christopher A ^a   Shaw, Jessica ^a   Zhao, Zack ^a   Reed, Robert A ^a  

^a MERCK RESEARCH LABORATORIES   (United States)

Author keywords

Degradation product quantitation; Extemporaneous; HPLC; Lisinopril; Method development; Method validation; Methyl paraben; Propyl paraben

Indexed keywords

4 HYDROXYBENZOIC ACID ESTER; CITRATE DISODIUM; DILUENT; LISINOPRIL; METHYL PARABEN; ORA SWEET; PROPYL PARABEN;

ANALYTIC METHOD; ARTICLE; CONCENTRATION (PARAMETERS); DRUG DETERMINATION; DRUG FORMULATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; VALIDATION PROCESS;

EID: 14644416498     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2004.11.021     Document Type: Article

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