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45. Current FDA policy on use of human-labeled drugs in animals. Teske RH J Am Vet Med Assoc; 1993 May; 202(10):1632-3;discussion 1634. PubMed ID: 8514570 [No Abstract] [Full Text] [Related]
46. FDA's regulation of prescription drug labeling: a role for implied preemption. Kendrick LC Food Drug Law J; 2007; 62(1):227-47. PubMed ID: 17444031 [No Abstract] [Full Text] [Related]
47. Implications for the FDA/Center for Veterinary Medicine (CVM). Geyer RE J Am Vet Med Assoc; 1993 May; 202(10):1718-23. PubMed ID: 8514592 [No Abstract] [Full Text] [Related]
52. A lesson from Melos. Owen JA Hosp Formul; 1979 Feb; 14(2):127. PubMed ID: 10240142 [No Abstract] [Full Text] [Related]
53. View from the Nation's Capital. FDA challenged successfully on its policies regarding good manufacturing practice inspections of medical drug and device manufacturers. Appler WD J Clin Psychopharmacol; 1987 Oct; 7(5):346-7. PubMed ID: 3680606 [No Abstract] [Full Text] [Related]
55. The patient package insert--health care provider's friend or foe? Hirsh HL Nurs Homes; 1979; 28(4):24-5. PubMed ID: 10283734 [No Abstract] [Full Text] [Related]
56. FDA commissioner discusses issues of concern to hospital pharmacists. Interview by William A. Zellmer. Goyan JE Am J Hosp Pharm; 1980 May; 37(5):738-40 contd. PubMed ID: 7386484 [No Abstract] [Full Text] [Related]
57. The health hazard of unlabeled ingredients in pharmaceuticals. Brown JL Pediatrics; 1984 Mar; 73(3):402-4. PubMed ID: 6701067 [No Abstract] [Full Text] [Related]
58. The issue of "generic" versus "trade" names. Taylor WJ Int Z Klin Pharmakol Ther Toxikol; 1969 Jan; 2(1):1-2. PubMed ID: 5798943 [No Abstract] [Full Text] [Related]