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Journal Abstract Search

113 related items for PubMed ID: 4762187

  • 1. Inconsistencies in rationale underlying official USP dissolution rate specifications for nitrofurantoin.
    Bates TR, Rosenberg HA, Tembo AV.
    J Pharm Sci; 1973 Dec; 62(12):2057-8. PubMed ID: 4762187
    [No Abstract] [Full Text] [Related]

  • 2. pH-dependent dissolution rate of nitrofurantoin from commercial suspensions, tablets, and capsules.
    Bates TR, Young JM, Wu CM, Rosenberg HA.
    J Pharm Sci; 1974 Apr; 63(4):643-5. PubMed ID: 4828728
    [No Abstract] [Full Text] [Related]

  • 3. Dissolution test acceptance sampling plans.
    Tsong Y, Hammerstrom T, Lin K, Ong TE.
    J Biopharm Stat; 1995 Jul; 5(2):171-83. PubMed ID: 7581426
    [Abstract] [Full Text] [Related]

  • 4. [Biologic availability of various formulas of nitrofurantoin in tablets].
    Frigerio G, Venier A.
    Boll Chim Farm; 1973 Jul; 112(6):416-21. PubMed ID: 4767643
    [No Abstract] [Full Text] [Related]

  • 5. Proceedings: The comparison of the bioavailabilities of commercial nitrofurantoin tablets.
    McGilveray IJ, Mattok GL, Hossie RD.
    Rev Can Biol; 1973 Jul; 32():Suppl:99-106. PubMed ID: 4777608
    [No Abstract] [Full Text] [Related]

  • 6. Collaborative study of the USP dissolution test for prednisone tablets with Apparatus 2.
    Cox DC, Furman WB.
    J Pharm Sci; 1984 May; 73(5):670-6. PubMed ID: 6737242
    [Abstract] [Full Text] [Related]

  • 7. Bioavailability of 14 nitrofurantoin products.
    Meyer MC, Slywka GW, Dann RE, Whyatt PL.
    J Pharm Sci; 1974 Nov; 63(11):1693-8. PubMed ID: 4427226
    [No Abstract] [Full Text] [Related]

  • 8. [In vitro and in vivo investigations with different nitrofurantoin formulations (author's transl)].
    Gladigau V, Gebhardt U.
    Arzneimittelforschung; 1978 Nov; 28(10):1771-8. PubMed ID: 582682
    [Abstract] [Full Text] [Related]

  • 9. AAPS/USP Workshop on Dissolution Calibration and Testing.
    Carrico CK.
    Pharm Res; 1996 Jan; 13(1):6-9. PubMed ID: 8668680
    [No Abstract] [Full Text] [Related]

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  • 13. Systematic error associated with apparatus 2 of the USP dissolution test III: limitations of calibrators and the USP suitability test.
    Cox DC, Furman WB, Thornton LK, Moore TW, Jefferson EH.
    J Pharm Sci; 1983 Aug; 72(8):910-3. PubMed ID: 6620145
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  • 14. A comparative study of BP and USP rotating basket dissolution apparatus.
    Smith WJ, Heaume PE, Hailey DM, Lea AR.
    J Pharm Pharmacol; 1985 Feb; 37(2):124-5. PubMed ID: 2858545
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  • 16. Letter: Utility of preparations of nitrofurantoin.
    N Engl J Med; 1974 Jun 20; 290(25):1436-7. PubMed ID: 4829566
    [No Abstract] [Full Text] [Related]

  • 17. Feasibility of biowaiver extension to biopharmaceutics classification system class III drug products: cimetidine.
    Jantratid E, Prakongpan S, Amidon GL, Dressman JB.
    Clin Pharmacokinet; 2006 Jun 20; 45(4):385-99. PubMed ID: 16584285
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  • 19. A study of bioavailabilities and dissolution rates of commercial tablets of nitrofurantoin.
    McGilveray IJ, Mattok GL, Hossie RD.
    J Pharm Pharmacol; 1971 Dec 20; 23():246S. PubMed ID: 4401504
    [No Abstract] [Full Text] [Related]

  • 20. Effect of batch age on potency and dissolution of levothyroxine sodium tablets: impact of BP and USP monograph differences on dissolution results.
    Abou-Taleb BA, Nounou MI, Khalafallah N, Khalil S.
    Drug Dev Ind Pharm; 2018 Nov 20; 44(11):1762-1769. PubMed ID: 29973090
    [Abstract] [Full Text] [Related]

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