Single dose pharmacokinetic equivalence study of two gabapentin preparations in healthy subjects

BACKGROUND: The current study was conducted to find out whether two oral preparations of 300 mg gabapentin (the test and reference capsules) were bioequivalent. SUBJECTS AND METHODS: This was a randomized, single-blind, crossover study under fasting condition, with a 7-day washout period, which incl...

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Detalles Bibliográficos
Autores principales: Tjandrawinata, Raymond R, Setiawati, Effi, Putri, Ratih Sofia Ika, Yunaidi, Danang Agung, Amalia, Fawzia, Susanto, Liana W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159312/
https://www.ncbi.nlm.nih.gov/pubmed/25214768
http://dx.doi.org/10.2147/DDDT.S69326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159312/
https://www.ncbi.nlm.nih.gov/pubmed/25214768
http://dx.doi.org/10.2147/DDDT.S69326

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