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USFDA "Unapproved Drugs: Drugs Marketed in the United States That Do Not Have Required FDA Approval." Web Page maintained by US Food and Drug Administration, Rockville, MD, 2009, http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/EnforcementActivitiesbyFDA/SelectedEnforcementActionsonUnapprovedDrugs/default.htm.
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USFDA "Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book)." Web Page maintained by US Food and Drug Administration, Rockville, MD, 2009, http://www.fda.gov/Drugs/InformationOnDrugs/ucm129662.htm.
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USFDA "Safe Use Initiative: Collaborating to Reduce Preventable Harm from Medications." Web Page maintained by US Food and Drug Administration, Silver Spring, MD, 2009, http://www.fda.gov/Drugs/DrugSafety/ucm187806.htm.
USFDA. "Topical Testosterone Gel Products (Marketed as AndroGel 1% and Testim 1%): Secondary Exposure of Children to Topical Testosterone Products." Drug Safety Newsletter 2009, 2(3):21-23.
USFDA "New FDA Web Page Lists Disposal Instructions for Select Medicines." Web Page maintained by US Food and Drug Administration, Rockville, MD, 2009, http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm186598.htm.
USFDA. 2009, "Labeling and Packaging Requirements for Controlled Substances." US Food and Drug Administration, Rockville, MD, Code of Federal Regulations, 21CFR1302, revised 1 April 2009, http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=1302&showFR=1
USFDA. "Human drugs and biologics: Categorical Exclusion for New Drug Applications where the Active Ingredient's Concentration at its Point of Entry to the Environment Is Predicted to Be below 1 part per billion." Federal Register 2009, 21 CFR Ch. I, � 25.31:252.
USFDA. 2009, "Importation of Active Pharmaceutical Ingredients (APIs) Requirements, [21 USC �353] Exemptions and Consideration for Diltiazem Xr 180 Mg Certain Drugs, Devices, and Biological Products." US Food and Drug Administration, Rockville, MD, FD&C Act: SEC. 503. [21 USC �353], http://www.fda.gov/RegulatoryInformation/Legislation/FederalFoodDrugandCosmeticActFDCAct/FDCActChapterVDrugsandDevices/ucm108068.htm.
USFDA "Medicines Recommended for Disposal by Flushing." Web Page maintained by US Food and Drug Administration, Rockville, MD, 2009 [revised March 2010], http://www.fda.gov/Drugs/ResourcesForYou/Consumers/BuyingUsingMedicineSafely/EnsuringSafeUseofMedicine/SafeDisposalofMedicines/ucm186187.htm#MEDICINES.
USFDA "Disposal by Flushing of Certain Unused Medicines: What You Should Know. List of Medicines Recommended for Disposal by Flushing." Web Page maintained by US Food and Drug Administration, Rockville, MD, 2009 [revised March 2010], http://www.fda.gov/Drugs/ResourcesForYou/Consumers/BuyingUsingMedicineSafely/EnsuringSafeUseofMedicine/SafeDisposalofMedicines/ucm186187.htm.
USFDA. 2010, "21 C.F.R.� 211.204 Returned drug products. Code of Federal Regulations, 21 C.F.R. Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals, Subpart K: Returned and Salvaged Drug Products." Food and Drug Diltiazem Xr 240 Mg Administration, Department of Health Diltiazem Er 240 Mg Caps and Human Services, Washington, DC, 1 pp; http://law.justia.com/us/cfr/title21/21-4.0.1.1.10.11.1.1.html.
USFDA. "FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals." US Food and Drug Administration, Silver Spring, MD, 28 June, 2010, 2 pp; available: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm217464.htm.
USFDA. "The Judicious Use of Medically Important Antimicrobial Drugs in Food-Producing Animals." US Food and Drug Administration, Center for Veterinary Medicine, Silver Spring, MD, # 209, 28 June, 2010, 19 pp; available: http://www.fda.gov/downloads/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/UCM216936.pdf.
USFDA. "Questions and Diltiazem Cd 300 Mg Answers on FDA's Draft Guidance on the Judicious Use of Medically Important Diltiazem Cd Dosage Antimicrobial Drugs in Food-Producing Animals." US Food and Drug Administration, Silver Spring, MD, 2010, 3 pp; available: http://www.fda.gov/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/ucm216939.htm.
USFDA. 2010, "21 C.F.R.� 211.208 Drug product salvaging. Code of Federal Buy Diltiazem Cd Regulations, 21 C.F.R. Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals, Subpart K: Returned and Salvaged Drug Products." Food and Drug Administration, Department of Health and Human Services, Washington, DC, 1 pp; http://law.justia.com/us/cfr/title21/21-4.0.1.1.10.11.1.1.html.
USFDA. "Statement for National Poison Prevention Week: FDA Committed to Addressing Growing National Overdose Problem." US Food and Drug Administration, Silver Spring, MD, 2010. 2 pp; http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm204962.htm.
USFDA "Medication Disposal: Questions and Answers." Web Page maintained by US Food and Drug Administration, Silver Spring, MD, 2010, http://www.fda.gov/Drugs/ResourcesForYou/Consumers/BuyingUsingMedicineSafely/EnsuringSafeUseofMedicine/SafeDisposalofMedicines/ucm186188.htm.
USFDA. ""Sexual Enhancement" Supplements Contained Viagra Analogue." US Food and Drug Administraiton, Maitland FL, 13 July, 2010. http://www.fda.gov/ICECI/EnforcementActions/WarningLetters/ucm215918.htm; http://tiny.cc/n14qv.
USFDA. "FDA Warns About Fraudulent Tamiflu: Fraudulent product is dangerous to patients allergic to penicillin." US Food and Drug Administration, Washington, DC, 17 June, 2010. 2 pp; http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm216148.htm; http://tiny.cc/9sg7a.
USFDA. "Buying Medicines Over the Internet." US Food and Drug Administration, Rockville, MD, 5 September, 2010. http://www.fda.gov/Drugs/ResourcesForYou/Consumers/BuyingUsingMedicineSafely/BuyingMedicinesOvertheInternet/default.htm.
USFDA "Triclosan: What Consumers Should Know." Web Page maintained by US Department of Health & Human Sciences, Washington, DC, 2010, http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm205999.htm.
USFDA. "Intelli Health Products, Issues an Expansion to All Lots of their Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements." US Department of Health and Human Services, US Food and Drug Administration, Silver Spring, MD, 2 December, 2010, 1 pp; available: http://www.fda.gov/Safety/Recalls/ucm235848.htm.
USFDA. "Considering Whether an FDA-Regulated Product Involves the Application of Nanotechnology Guidance for Industry. DRAFT GUIDANCE. This guidance document is being distributed for comment purposes only." U.S. Department of Health & Human Services, U.S. Food and Drug Administration, Silver Spring, MD, 2010, 4 pp; available: http://www.fda.gov/RegulatoryInformation/Guidances/ucm257698.htm.
USFDA. "FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals." US Food and Drug Administration, US Department of Health and Human Services, Silver Spring, MD, 28 June, 2010. 2 pp; http://www.fda.gov/newsevents/newsroom/pressannouncements/ucm217464.htm.
USFDA. "Withdrawal of Notices Diltiazem Er 360 Mg of Opportunity for a Hearing; Penicillin and Tetracycline Used in Animal Feed." Federal Register 2011, 76(246):79697-79701.
USFDA. "How to dispose of unused medicines." Consumer Health Information, US Food and Drug Administration, Rockville, MD, 14 October, 2012. 2 pp; http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm101653.htm.
USFDA. "Agency working with animal, drug and medical communities to promote judicious antimicrobial use." US Food and Drug Administration, US Department of Health and Human Services, Silver Spring, MD, 11 April, 2012. 2 pp; http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm299802.htm.
USFDA. "Guidance for Industry: The Judicious Use of Medically Important Antimicrobial Drugs in Food-Producing Animals." US Food and Drug Administration and Center for Veterinary Medicine, US Department of Health and Human Services, Rockville, MD, Docket No. FDA-2010-D-0094, 13 April, 2012. 26 pp; http://www.fda.gov/downloads/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/UCM216936.pdf.
USFDA. "FDA's Strategy on Antimicrobial Resistance - Questions and Answers." US Food and Drug Administration, US Department of Health and Human Services, Silver Spring, MD, 2012. 3 pp; http://www.fda.gov/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/ucm216939.htm.
USFDA "FDA Reminds the Public about the Potential for Life-Threatening Harm from Accidental Exposure to Fentanyl Transdermal Systems (?Patches�)." Web Page maintained by U.S. Food and Drug Administration, Silver Spring, MD, 2012, http://www.fda.gov/Drugs/DrugSafety/ucm300747.htm.
USFDA. "Fentanyl Patch Can Be Deadly to Children." FDA Consumer Health Information/U.S. Food and Drug Administration 2012:1-2.
USFDA. "Using Innovative Technologies and Other Conditions of Safe Use to Expand Drug Products Considered Nonprescription." Federal Register 2012, 77(39):12059-12062.
USFDA. "Draft Guidance for Industry: Safety of Nanomaterials in Cosmetic Products." U.S. Department of Health and Human Services, Food and Drug Administration, Office of Foods, Center for Food Safety and Applied Nutrition, Rockville, MD, April, 2012, 24 pp; available: http://www.fda.gov/Cosmetics/GuidanceComplianceRegulatoryInformation/GuidanceDocuments/ucm300886.htm.
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USFDA (Leslie Kux). "Guidance for Industry: Residual Drug in Transdermal and Related Drug Delivery Systems." Food and Drug Administration, Center for Drug Evaluation and Research (CDER) and Office of Pharmaceutical Science, U.S. Department of Health and Human Services, Rockville, MD, 2010. 5 pp; http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM220796.pdf; http://www.federalregister.gov/articles/2010/08/03/2010-19041/draft-guidance-for-industry-on-residual-drug-in-transdermal-and-related-drug-delivery-systems.
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USGAO. "Offshore Marine Aquaculture, Multiple administrative and environmental issues need to be addressed in establishing a US regulatory framework." US Government Accountability Office, Washington, DC, GAO-08-594, May, 2008. 54 pp.
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USGAO. "Herbal Dietary Supplements: Examples of Deceptive or Questionable Marketing Practices and Potentially Dangerous Advice." US Government Accountability Office (GAO), Washington, DC, GAO-10-662T, 26 May, 2010, 28 pp; available: http://www.gao.gov/new.items/d10662t.pdf.
USGAO. "Antibiotic Resistance: Data Gaps Will Remain Despite HHS Taking Steps to Improve Monitoring." US Government Accountability Office (GAO), Washington, DC, 1 June, 2011, 66 pp; available: http://www.gao.gov/products/GAO-11-406; http://www.gao.gov/new.items/d11406.pdf.
USGAO. "Safe Drinking Water Act: EPA Should Improve Implementation of Requirements on Whether to Regulate Additional Contaminants." US Government Accountability Office (GAO), Washington, DC, 27 May, 2011, 146 pp; available: http://www.gao.gov/new.items/d11254.pdf.
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USGS, MPCA, St. Cloud State University, and University of St. Thomas "Relative contributions of selected endocrine active chemicals and pharmaceuticals from wastewater treatment plant effluent and other sources to Minnesota surface waters v Implications for aquatic communities." Web Page maintained by US Geological Survey, St. Paul, MN, 2010, http://mn.water.usgs.gov/projects/EACWWTP/index.html.
Uslu M� and Akmehmet BalcIoglu I. "Comparison of the ozonation and Fenton process performances for the treatment of antibiotic containing manure." Science of the Total Environment 2009, 407(11):3450-3458; doi:10.1016/j.scitotenv.2009.01.045.
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