메뉴 건너뛰기




Volumn 3, Issue 2, 2010, Pages 37-43

Bioequivalence of the 4-mg Oral Granules and Chewable Tablet Formulations of Montelukast

Author keywords

Bioequivalence; Montelukast; Pediatric Formulations; Pharmacokinetics

Indexed keywords

MONTELUKAST;

EID: 77954364630     PISSN: None     EISSN: 17535174     Source Type: Journal    
DOI: 10.1111/j.1753-5174.2010.00029.x     Document Type: Article
Times cited : (9)

References (7)
  • 2
    • 17844373539 scopus 로고    scopus 로고
    • Montelukast dose selection in children ages 2 to 5 years: Comparison of population pharmacokinetics between children and adults
    • Knorr B, Nguyen HH, Kearns GL, Villaran C, Boza ML, Reiss TF. Montelukast dose selection in children ages 2 to 5 years: Comparison of population pharmacokinetics between children and adults. J Clin Pharmacol 2001, 41:612-9.
    • (2001) J Clin Pharmacol , vol.41 , pp. 612-619
    • Knorr, B.1    Nguyen, H.H.2    Kearns, G.L.3    Villaran, C.4    Boza, M.L.5    Reiss, T.F.6    et al7
  • 3
    • 0033306919 scopus 로고    scopus 로고
    • Montelukast dose selection in 6- to 14-year-olds: Comparison of single-dose pharmacokinetics in children and adults
    • Knorr B, Larson P, Nguyen HH, Holland S, Reiss TF, Chervinsky P. Montelukast dose selection in 6- to 14-year-olds: Comparison of single-dose pharmacokinetics in children and adults. J Clin Pharmacol 1999, 39:786-93.
    • (1999) J Clin Pharmacol , vol.39 , pp. 786-793
    • Knorr, B.1    Larson, P.2    Nguyen, H.H.3    Holland, S.4    Reiss, T.F.5    Chervinsky, P.6    et al7
  • 4
    • 77954375421 scopus 로고    scopus 로고
    • Food and Drug Administration Center for Drug Evaluation and Research (CDER) Guidance for industry: Bioavailability and bioequivalence studies for orally administered drug products-General considerations
    • US Department of Health and Human Services
    • Food and Drug Administration Center for Drug Evaluation and Research (CDER) Guidance for industry: Bioavailability and bioequivalence studies for orally administered drug products-General considerations. 2000, US Department of Health and Human Services
    • (2000)
  • 5
    • 77954350156 scopus 로고    scopus 로고
    • Evaluation of Medicines for Human Use, Committee for Proprietary Medicinal Products (CPMP) Note for guidance on the investigation of bioavailability and bioequivalence
    • European Agency for the Evaluation of Medicinal Products
    • Evaluation of Medicines for Human Use, Committee for Proprietary Medicinal Products (CPMP) Note for guidance on the investigation of bioavailability and bioequivalence. 2000, European Agency for the Evaluation of Medicinal Products
    • (2000)
  • 6
    • 0002372484 scopus 로고
    • Determination of MK-0476 in human plasma by liquid chromatography
    • Amin RD, Cheng H, Rogers JD. Determination of MK-0476 in human plasma by liquid chromatography. J Pharm Biomed Anal 1995, 40:277-80.
    • (1995) J Pharm Biomed Anal , vol.40 , pp. 277-280
    • Amin, R.D.1    Cheng, H.2    Rogers, J.D.3
  • 7
    • 77954354641 scopus 로고    scopus 로고
    • Food and Drug Administration Center for Drug Evaluation and Research (CDER) Guidance for industry: Food-effect bioavailability and fed bioequivalence studies
    • US Department of Health and Human Services
    • Food and Drug Administration Center for Drug Evaluation and Research (CDER) Guidance for industry: Food-effect bioavailability and fed bioequivalence studies. 2002, US Department of Health and Human Services
    • (2002)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.