Use of Proprietary Names by Prescribers for Generic Products-Reference-Cited by-同舟云学术

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Use of Proprietary Names by Prescribers for Generic Products

Published:2018-03 Issue:2 Volume:52 Page:256-260
ISSN:2168-4790
Container-title:Therapeutic Innovation & Regulatory Science
language:en
Short-container-title:Ther Innov Regul Sci

Author:

Borders-Hemphill Vicky,Chan Irene Z.,Brown Katelyn,Rider Briana,Taylor Kellie,Chai Grace

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Link

http://link.springer.com/content/pdf/10.1177/2168479017723399.pdf

Reference13 articles.

1. Food and Drug Administration. Abbreviated New Drug Application (ANDA): generics. http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/AbbreviatedNewDrugApplicationANDAGenerics/. Accessed March 2015.

2. Food and Drug Administration. Guidance for industry. Best practices in developing proprietary names for drugs. http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM398997.pdf. Accessed April 20, 2015.

3. ISMP Medication Safety Alert! April 19, 2000;(5)8.

4. Institute for Safe Medication Practices. ISMP’s list of confused drug names. https://www.ismp.org/tools/confuseddrugnames.pdf. Accessed April 27, 2015.

5. ISMP Medication Safety Alert! August 14, 2008;(13)19.

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