Development and Validation of RP-HPLC method for the determination of Ganciclovir in bulk drug and its formulations

International Journal of Pharma and Bio Sciences

Volumn 1, Issue 2, 2010, Pages

  Sarsambi, Prakash S ^a   Sonawane, Abhay ^a   Faheem, Abdul ^a  

^a HKES's College of pharmacy   (India)

Author keywords

Acyclovir; Ganciclovir (GCV); Internal standard; RP HPLC

Indexed keywords

ACICLOVIR; GANCICLOVIR; METHANOL; TRIFLUOROACETIC ACID;

ACCURACY; ARTICLE; CONTROLLED STUDY; DRUG DETERMINATION; DRUG STRUCTURE; LIMIT OF DETECTION; LIMIT OF QUANTITATION; PROCESS DEVELOPMENT; PROCESS OPTIMIZATION; QUALITY CONTROL; QUANTITATIVE ANALYSIS; REPRODUCIBILITY; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SENSITIVITY AND SPECIFICITY; SEPARATION TECHNIQUE; TEMPERATURE DEPENDENCE; VALIDATION PROCESS;

EID: 84455202121     PISSN: None     EISSN: 09756299     Source Type: Journal    
DOI: None     Document Type: Article

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