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Volumn 47, Issue 11, 1997, Pages 1236-1241
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Investigation into the bioequivalence of a new allopurinol tablet formulation compared with a standard preparation;UNTERSUCHUNGEN ZUR BIOAQUIVALENZ EINER NEUEN ALLOPURINOL-TABLETTENFORMULIERUNG IM VERGLEICH ZU EINER REFERENZFORMULIERUNG
a b c a
a
Galmed GmbH
(Germany)
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Author keywords
Allo 300 von ct; Allopurinol, bioequivalence, clinical studies; Antigout agent; CAS 315 30 0; Oxipurinol
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Indexed keywords
ALLOPURINOL;
OXIPURINOL;
ANTIMETABOLITE;
ADULT;
ARTICLE;
BIOEQUIVALENCE;
CONTROLLED STUDY;
DRUG BLOOD LEVEL;
DRUG DETERMINATION;
DRUG SAFETY;
FEMALE;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
HUMAN EXPERIMENT;
MALE;
NORMAL HUMAN;
ORAL DRUG ADMINISTRATION;
TABLET FORMULATION;
ULTRAVIOLET SPECTROPHOTOMETRY;
AREA UNDER THE CURVE;
BLOOD;
CLINICAL TRIAL;
COMPARATIVE STUDY;
CROSSOVER PROCEDURE;
PHARMACOKINETICS;
RANDOMIZED CONTROLLED TRIAL;
ADULT;
ALLOPURINOL;
ANTIMETABOLITES;
AREA UNDER CURVE;
CROSS-OVER STUDIES;
FEMALE;
HUMANS;
MALE;
OXYPURINOL;
THERAPEUTIC EQUIVALENCY;
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EID: 0031262190
PISSN: 00044172
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (5)
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References (14)
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