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PUBMED FOR HANDHELDS

Journal Abstract Search


529 related items for PubMed ID: 19112682

  • 21. Labeling of diphenhydramine-containing drug products for over-the-counter human use. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Dec 02; 67(235):72555-9. PubMed ID: 12474879
    [Abstract] [Full Text] [Related]

  • 22. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Aug 27; 63(166):45716-7. PubMed ID: 10182694
    [Abstract] [Full Text] [Related]

  • 23. Skin protectant drug products for over-the-counter human use; final monograph. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jun 04; 68(107):33362-81. PubMed ID: 12785379
    [Abstract] [Full Text] [Related]

  • 24. Amended economic impact analysis of final rule requiring use of labeling on natural rubber containing devices--FDA. Final rule; amended economic analysis statement.
    Fed Regist; 1998 Sep 22; 63(183):50660-704. PubMed ID: 10185803
    [Abstract] [Full Text] [Related]

  • 25. Amendment to the current good manufacturing practice regulations for finished pharmaceuticals. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Dec 04; 72(232):68064-70. PubMed ID: 18064770
    [Abstract] [Full Text] [Related]

  • 26. Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; policies, requirements, and administrative procedures; delay of effective date; reopening of administrative record. Food and Drug Administration, HHS. Final rule; delay of effective date; reopening of administrative record.
    Fed Regist; 2000 May 03; 65(86):25639-41. PubMed ID: 11010689
    [Abstract] [Full Text] [Related]

  • 27. Amended economic impact analysis of final rule requiring use of labeling on natural rubber containing devices--FDA. Final rule; amended economic analysis statement.
    Fed Regist; 1998 Aug 31; 63(168):46171-4. PubMed ID: 10182698
    [Abstract] [Full Text] [Related]

  • 28. Food labeling: health claims; calcium consumption by adolescents and adults, bone density and the risk of fractures--FDA. Interim final rule.
    Fed Regist; 1998 Jun 22; 63(119):34101-4. PubMed ID: 10180287
    [Abstract] [Full Text] [Related]

  • 29. Supplemental applications proposing labeling changes for approved drugs, biologics, and medical devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Aug 22; 73(164):49603-10. PubMed ID: 18958946
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. Antiperspirant drug products for over-the-counter human use; final monograph. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jun 09; 68(110):34273-93. PubMed ID: 12795305
    [Abstract] [Full Text] [Related]

  • 32. Pediculicide drug products for over-the-counter human use; amendment of final monograph. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 31; 68(250):75414-8. PubMed ID: 14986677
    [Abstract] [Full Text] [Related]

  • 33. Foreign establishment registration and listing. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Nov 27; 66(228):59138-61. PubMed ID: 11776289
    [Abstract] [Full Text] [Related]

  • 34. Food labeling: health claims; zinc and the body's ability to fight infection and heal wounds in adults--FDA. Interim final rule.
    Fed Regist; 1998 Jun 22; 63(119):34112-5. PubMed ID: 10180291
    [Abstract] [Full Text] [Related]

  • 35. Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; policies, requirements, and administrative procedures. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Dec 03; 64(232):67720-63. PubMed ID: 11010665
    [Abstract] [Full Text] [Related]

  • 36. Investigational new drug applications; clinical holds; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Dec 14; 63(239):68710-2. PubMed ID: 10187560
    [Abstract] [Full Text] [Related]

  • 37. Food labeling: health claims; vitamin K and promotion of proper blood clotting and improvements in bone health in adults--FDA. Interim final rule.
    Fed Regist; 1998 Jun 22; 63(119):34115-7. PubMed ID: 10180292
    [Abstract] [Full Text] [Related]

  • 38. Labeling requirements for systemic antibacterial drug products intended for human use. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Feb 06; 68(25):6062-81. PubMed ID: 12577966
    [Abstract] [Full Text] [Related]

  • 39. Conforming regulations regarding removal of section 507 of the Federal Food, Drug, and Cosmetic Act; confirmation of effective date. Food and Drug Administration, HHS. Direct final rule; confirmation of effective date.
    Fed Regist; 1999 May 17; 64(94):26657. PubMed ID: 10558515
    [Abstract] [Full Text] [Related]

  • 40. Requirements for submission of labeling for human prescription drugs and biologics in electronic format. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 11; 68(238):69009-20. PubMed ID: 14672084
    [Abstract] [Full Text] [Related]


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