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PUBMED FOR HANDHELDS

Journal Abstract Search

247 related items for PubMed ID: 10169832

  • 1. Content and format of labeling for human prescription drugs; pregnancy labeling; public hearing--FDA. Notice of public hearing; request for comments.
    Fed Regist; 1997 Jul 31; 62(147):41061-3. PubMed ID: 10169832
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  • 2. 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]

  • 3. Requirements on content and format of labeling for human prescription drug and biological products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Jan 24; 71(15):3921-97. PubMed ID: 16479698
    [Abstract] [Full Text] [Related]

  • 4. Content and format of labeling for human prescription drug and biological products; requirements for pregnancy and lactation labeling. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2014 Dec 04; 79(233):72063-103. PubMed ID: 25509060
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  • 9. The new FDA pregnancy labeling requirements for drugs.
    Frederiksen MC.
    J Midwifery Womens Health; 2011 Dec 04; 56(3):303-7. PubMed ID: 21535377
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  • 11. Over-the-counter human drugs; labeling requirements. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Mar 17; 64(51):13254-303. PubMed ID: 10557606
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  • 12. Maternal characteristics associated with pregnancy exposure to FDA category C, D, and X drugs in a Canadian population.
    Yang T, Walker MC, Krewski D, Yang Q, Nimrod C, Garner P, Fraser W, Olatunbosun O, Wen SW.
    Pharmacoepidemiol Drug Saf; 2008 Mar 17; 17(3):270-7. PubMed ID: 18181228
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  • 13. FDA proposes more stringent pediatric-use labeling of prescription drug products.
    Am J Hosp Pharm; 1993 Jan 17; 50(1):13, 16. PubMed ID: 8427271
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  • 14. Progestational drug products for human use; requirements for labeling directed to the patient. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Nov 16; 64(220):62110-2. PubMed ID: 11010691
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  • 15. Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment.
    Fed Regist; 2000 Jan 03; 65(1):7-9. PubMed ID: 11010625
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  • 17. Prescription drug use in pregnancy.
    Andrade SE, Gurwitz JH, Davis RL, Chan KA, Finkelstein JA, Fortman K, McPhillips H, Raebel MA, Roblin D, Smith DH, Yood MU, Morse AN, Platt R.
    Am J Obstet Gynecol; 2004 Aug 03; 191(2):398-407. PubMed ID: 15343213
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  • 18. Drug labeling; sodium labeling for over-the-counter drugs. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Nov 29; 69(228):69278-80. PubMed ID: 15570675
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  • 19. 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
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  • 20. Sunscreen drug products for over-the-counter human use; final monograph. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 May 21; 64(98):27666-93. PubMed ID: 10558542
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