Randomized crossover studies of the bioequivalence of two commercially available ciprofloxacin after administration of a single oral dose in healthy volunteers

HIV and AIDS Review

Volumn 5, Issue 1, 2006, Pages 20-29

  Nesseem, Demiana Ibrahim ^a,b   Abou Taleb, Nisserin F ^a   Abou Basha, Laila ^a   Molokhia, Abdulla M ^a  

^a NATIONAL ORGANIZATION FOR DRUG CONTROL AND RESEARCH NODCAR   (Egypt)

^b NONE   (Egypt)

Author keywords

Bioequivalence; Ciprofloxacin; Dissolution; Pharmacokinetics

Indexed keywords

CIPROCIN; CIPROFLOXACIN;

ADULT; AREA UNDER THE CURVE; ARTICLE; BIOEQUIVALENCE; CENTRIFUGATION; CLINICAL TRIAL; CONFIDENCE INTERVAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CROSSOVER PROCEDURE; DRUG ABSORPTION; DRUG BIOAVAILABILITY; DRUG BLOOD LEVEL; DRUG HALF LIFE; DRUG RELEASE; DRUG SOLUBILITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN EXPERIMENT; IN VITRO STUDY; MALE; MEAN RESIDENCE TIME; NORMAL HUMAN; RANDOMIZED CONTROLLED TRIAL; SINGLE DRUG DOSE; STATISTICAL SIGNIFICANCE; TABLET FORMULATION; VOLUNTEER;

EID: 33744970100     PISSN: 17301270     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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