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Order phenergan over the counter for non-oral use, even in the presence of a physician. We oppose the expansion or extension of non-labeled products market for these medications to include the FDA's broad authority to require labeling and control its safety standards. We support the FDA's continued emphasis on best value prescription-only drug for each consumer to ensure access safer, traditional treatment in order to expand and maintain access medication that has more proven benefits than the generic alternatives currently available. We believe that the pharmaceutical industry should be able to make a reasonable profit by selling branded drugs for a longer period of time in the marketplace. This has prompted industry to reduce the duration of life patented drugs, and to try get as many patents out possible, leaving consumers with cheaper alternatives that do not have the name and patent of original patentholder. In 2012 the United States will need a new generation of drugs, capable treating more and different diseases, to help manage our growing population, increase competitiveness and extend lives. The new Sildenafil dosage for pah drugs will require development processes in manufacturing facilities, but also new knowledge and management skills. To the extent that this requires innovation, it should be encouraged and incentivized. To the extent that it takes place within the current system of intellectual property and access price protections, we have concerns as well regarding incentives for this innovation new drugs. We do, however, recognize that some of these steps have already been taken through the promotion of non-patented pharmaceuticals. Our position represents the most current medical and financial data which we feel is the best position for its industry. We believe that all manufacturers of medicines should be able to compete fairly on the basis of quality and performance, we believe that health care consumers have a right to get affordable medicines. This issue is not a fight over the details of prescription drug system; it is a battle over the fact that we continue to use prescriptions for the vast majority of our healthcare. While some believe that one of the unintended consequences to prescription drug market is the reduction of generic competition through patent monopolies, this is not true. Conclusion and Recommendations The American Medical Association Recommendation We recommend that the American Medical Association (AMA) adopt the Pharmaceutical Affairs Committee's position that all drugs must clearly and visibly display the generic name when these labels apply, and follow the same procedure when a generic manufacturer approaches the USPTO to make a generic label application for drug or product name. We believe this will greatly reduce the cost and inconvenience associated with receiving products that are not marked "Pharmaceutical Advantage or Generic." We also note that many products have the generic name on packaging but may not display the generic name on package. Our Recommendation is based on the position of AMA Council on Science and Public Health (2009): "The role of the AMA Council on Science and Public Health, in Phenergan 25mg $114.84 - $0.43 Per pill the AMA's work to protect public health, is examine how information in a drug label might influence health decisions or behaviors, and how industry might influence the public regarding its treatment of disease. Drug labels should disclose all relevant information, including non-specific, generic information. If a manufacturer requests, the AMA should review how label disclosure might be expanded to disclose generic information." Our Recommendation is based on the work of International Life Sciences Institute (ILSI) Task Force on Medicinal Drugs (2009) Recommendation We recommend that the International Life Sciences Institute recommend that, in addition to listing all known active ingredients and other data regarding a drug, the manufacturer should include a summary which includes information regarding the other active ingredients. In many cases, this information may be critical and should included. This will help ensure consistent and adequate disclosure of other active ingredients in individual products, and will enable adequate use of.

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