A validated stability-indicating UPLC method for desloratadine and its impurities in pharmaceutical dosage forms

Journal of Pharmaceutical and Biomedical Analysis

Volumn 51, Issue 3, 2010, Pages 736-742

  Rao, Dantu Durga ^a,b   Satyanarayana, N V ^a   Malleswara Reddy, A ^a   Sait, Shakil S ^a   Chakole, Dinesh ^a   Mukkanti, K ^b  

^a DR REDDY'S LABORATORIES LTD   (India)

^b JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY   (India)

Author keywords

Desloratadine; Development; Impurities; Stability indicating; UPLC; Validation

Indexed keywords

DESLORATADINE; SOLVENT;

ACCURACY; ARTICLE; DEGRADATION; DRUG DETERMINATION; DRUG DOSAGE FORM; DRUG IMPURITY; DRUG PURITY; DRUG STABILITY; DRUG STRUCTURE; HYDROLYSIS; MASS SPECTROMETRY; OXIDATIVE STRESS; PHOTOLYSIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REVERSED PHASE LIQUID CHROMATOGRAPHY; REVERSED PHASE ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY; SEPARATION TECHNIQUE; TABLET FORMULATION; VALIDATION PROCESS;

CHEMISTRY, PHARMACEUTICAL; CHROMATOGRAPHY, LIQUID; DOSAGE FORMS; DRUG CONTAMINATION; DRUG STABILITY; LORATADINE; PHARMACEUTICAL SOLUTIONS;

EID: 70449112651     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2009.09.016     Document Type: Article

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