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Volumn 4, Issue 1, 2013, Pages 621-638
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Development of stability indicating method for validation of Losartan potassium and hydrochlorothiazide drugs in solid dosage form by RP-HPLC
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Author keywords
Antihypertensive; Chromatograms; Quantitated; Resolution; Theoretical plates
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Indexed keywords
HYDROCHLOROTHIAZIDE;
LOSARTAN POTASSIUM;
ACCURACY;
ARTICLE;
CHEMICAL PARAMETERS;
CONCENTRATION (PARAMETERS);
CONTROLLED STUDY;
DRUG DETERMINATION;
DRUG EFFICACY;
DRUG POTENCY;
DRUG QUALITY;
DRUG SAFETY;
DRUG SPECIFICITY;
DRUG STABILITY;
DRUG STRUCTURE;
FLOW RATE;
LIMIT OF DETECTION;
LIMIT OF QUANTITATION;
LINEARITY;
PROCESS DEVELOPMENT;
RANGE;
REPRODUCIBILITY;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
ROBUSTNESS;
VALIDATION PROCESS;
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EID: 84879668705
PISSN: None
EISSN: 09756299
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (3)
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References (10)
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