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PUBMED FOR HANDHELDS

Journal Abstract Search


677 related items for PubMed ID: 10317245

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. The FDA's generic-drug approval process: similarities to and differences from brand-name drugs.
    Kefalas CH, Ciociola AA.
    Am J Gastroenterol; 2011 Jun; 106(6):1018-21. PubMed ID: 21637264
    [No Abstract] [Full Text] [Related]

  • 23. The debate over substitution policy. Its evolution and scientific basis.
    Schwartz LL.
    Am J Med; 1985 Aug 23; 79(2B):38-44. PubMed ID: 3898831
    [Abstract] [Full Text] [Related]

  • 24. Generic low-molecular-weight heparins: some practical considerations.
    Fareed J, Leong WL, Hoppensteadt DA, Jeske WP, Walenga J, Wahi R, Bick RL.
    Semin Thromb Hemost; 2004 Dec 23; 30(6):703-13. PubMed ID: 15630677
    [Abstract] [Full Text] [Related]

  • 25. New York State and drug lists: a history of confusion.
    Stetler CJ.
    Med Mark Media; 1978 Sep 23; 13(9):36, 38, 40 passim. PubMed ID: 10316687
    [No Abstract] [Full Text] [Related]

  • 26. Current issues in the pioneer versus generic drug wars.
    Safir PO.
    Food Drug Law J; 1995 Sep 23; 50(2):335-9. PubMed ID: 10343002
    [No Abstract] [Full Text] [Related]

  • 27. Brand-name drug manufacturers risk antitrust violations by slowing generic production through patent layering.
    Paine CS.
    Seton Hall Law Rev; 2003 Sep 23; 33(2):479-510. PubMed ID: 12715807
    [No Abstract] [Full Text] [Related]

  • 28. Thalidomide and beyond: some recommendations regarding public policies toward the ethical drug industry.
    Schifrin LG.
    Int J Health Serv; 1974 Sep 23; 4(1):147-55. PubMed ID: 4829893
    [No Abstract] [Full Text] [Related]

  • 29.
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  • 30.
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  • 31. Benefits and liabilities of generic prescribing.
    Lee AM.
    W V Med J; 1972 Jun 23; 68(6):161-6. PubMed ID: 4504384
    [No Abstract] [Full Text] [Related]

  • 32.
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  • 33. Therapeutic equivalents in clinical practice.
    Benson MD.
    Int J Fertil Womens Med; 2001 Jun 23; 46(2):89-94. PubMed ID: 11374660
    [Abstract] [Full Text] [Related]

  • 34. Generic drugs and the prescribing physician.
    Nightingale SL, Morrison JC.
    JAMA; 1987 Sep 04; 258(9):1200-4. PubMed ID: 3626003
    [Abstract] [Full Text] [Related]

  • 35. United States Food and Drug Administration requirements for approval of generic drug products.
    Meyer MC.
    J Clin Psychiatry; 2001 Sep 04; 62 Suppl 5():4-9; discussion 23-4. PubMed ID: 11305846
    [Abstract] [Full Text] [Related]

  • 36. Assuring total drug quality.
    Simmons HE.
    J Am Pharm Assoc; 1973 Feb 04; 13(2):96-8. PubMed ID: 4686621
    [No Abstract] [Full Text] [Related]

  • 37. Information that brand-name companies do not tell us.
    Marcoux AW.
    Drug Intell Clin Pharm; 1987 Mar 04; 21(3):296-7. PubMed ID: 3569035
    [No Abstract] [Full Text] [Related]

  • 38. Meta-analysis for bioequivalence review.
    Chow SC, Liu J.
    J Biopharm Stat; 1997 Mar 04; 7(1):97-111. PubMed ID: 9056591
    [Abstract] [Full Text] [Related]

  • 39. Generic vs. brand name drugs--patients, pharmacists, physicians: caught in the middle.
    Felch WC.
    Internist; 1979 May 04; 20(4):3-5. PubMed ID: 10242131
    [No Abstract] [Full Text] [Related]

  • 40. Regulatory aspects of parenteral drugs.
    Jennings J.
    Bull Parenter Drug Assoc; 1972 May 04; 26(2):53-7. PubMed ID: 5012204
    [No Abstract] [Full Text] [Related]


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