Single dose study of the bioequivalence of two sustained-release theophylline formulations

Arzneimittel-Forschung/Drug Research

Volumn 48, Issue 3, 1998, Pages 259-262

  Contreras, Jiovanna ^a,b   Pérez, Néstor ^a   González, Raysa ^a   Ontivero, Elio ^a   López, Mireye ^a  

^a Department of Chemistry   (Cuba)

^b NATL CENTER FOR SCIENTIFIC RESEARCH   (Cuba)

Author keywords

Antiasthmatics; Bioequivalence; CAS 58 55 9; Clinical studies; Controfilina ; Theophylline

Indexed keywords

THEOPHYLLINE;

ADULT; AREA UNDER THE CURVE; ARTICLE; BIOEQUIVALENCE; CLINICAL TRIAL; CONTROLLED STUDY; DRUG BLOOD LEVEL; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN EXPERIMENT; SUSTAINED RELEASE PREPARATION;

ADULT; ANTI-ASTHMATIC AGENTS; AREA UNDER CURVE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DELAYED-ACTION PREPARATIONS; HUMANS; INDICATORS AND REAGENTS; MALE; THEOPHYLLINE; THERAPEUTIC EQUIVALENCY;

EID: 0031895348     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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