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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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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4159312/ https://ncbi.nlm.nih.gov/pubmed/25214768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DDDT.S69326 |
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