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PUBMED FOR HANDHELDS

Journal Abstract Search


165 related items for PubMed ID: 11010656

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  • 7. Erythrityl tetranitrate; drug efficacy study implementation; revocation of exemption; opportunity for a hearing--FDA. Notice.
    Fed Regist; 1998 Jun 23; 63(120):34188-90. PubMed ID: 10180293
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  • 12. Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices--FDA. Final rule.
    Fed Regist; 1998 Nov 20; 63(224):64556-88. PubMed ID: 10339052
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  • 14. Applications for Food and Drug Administration approval to market a new drug; postmarketing reports; reporting information about authorized generic drugs. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Sep 29; 73(189):56487-91. PubMed ID: 18985960
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  • 16. Digoxin products for oral use; revocation of conditions for marketing. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Jun 26; 67(123):42992-7. PubMed ID: 12120661
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  • 17. 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
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  • 19. Delegations of authority and organization; new drug applications--Food and Drug Administration. Final rule.
    Fed Regist; 1982 Jun 22; 47(120):26822-3. PubMed ID: 10255868
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