A stability indicating LC method for Rivastigmine hydrogen tartrate

Journal of Pharmaceutical and Biomedical Analysis

Volumn 37, Issue 1, 2005, Pages 57-63

  Rao, B Mallikarjuna ^a   Srinivasu, M K ^a   Kumar, K Praveen ^a   Bhradwaj, Neelu ^a   Ravi, R ^a   Mohakhud, Pradeep K ^a   Reddy, G Om ^a   Kumar, P Rajender ^a  

^a DR REDDY'S LABORATORIES LTD   (India)

Author keywords

Alzheimer's disease; Forced degradation; Pharmaceutical dosage form; Rivastigmine hydrogen tartrate; RPLC; Solution and mobile phase stability; Validation

Indexed keywords

3 (1 DIMETHYLAMINOETHYL)PHENOL; ACETONITRILE; HYDROCHLORIC ACID; HYDROGEN PEROXIDE; PHENOL DERIVATIVE; RIVASTIGMINE; SODIUM HYDROXIDE; UNCLASSIFIED DRUG;

ACCURACY; AQUEOUS SOLUTION; ARTICLE; DRUG IMPURITY; EXTRACTION; HEATING; INSTRUMENT; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REVERSED PHASE LIQUID CHROMATOGRAPHY; ULTRAVIOLET RADIATION; VALIDATION PROCESS;

CHROMATOGRAPHY, LIQUID; DRUG STABILITY; PHENYLCARBAMATES;

EID: 12344324779     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2004.09.041     Document Type: Article

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