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Generics Act of 1988

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Republic of the Philippines CONGRESS OF THE PHILIPPINES Metro Manila Second Regular Session Begun and held in Metro Manila, on Monday, the twenty-fifth day of July, nineteen hundred and eighty-eight [ REPUBLIC ACT NO. 6675 ] AN ACT TO PROMOTE, REQUIRE AND ENSURE THE PRODUCTION OF AN ADEQUATE SUPPLY, DISTRIBUTION, USE AND ACCEPTANCE OF DRUGS AND MEDICINES IDENTIFIED BY THEIR GENERIC NAMES Be it enacted by the Senate and House Representatives of the Philippines in Congress assembled: SECTION 1. Title – This Act shall be known as the Generics Act of 1988 SECTION 2. Statement of Policy – It is hereby declared the policy of the State: To promote, encourage and require the use of generic terminology in the importation, manufacture, distribution, marketing, advertising and promotion, prescription and dispensing of drugs; To ensure the adequate supply of drugs with generic names at the lowest possible cost and endeavor to make them available for free to indigent patients; To encourage the extensive use of drugs with generic names through a rational system of procurement and distribution; To emphasize the scientific basis for the use of drugs, in order that health professionals may become more aware and cognizant of their therapeutic effectiveness; and To promote drug safety by minimizing duplication in medications and/or use of drugs with potentially adverse drug interactions. SECTION 3. Definition of Terms – The following terms are herein defined for purposes of this Act: (1) "Generic Name or Generic Terminology" is the identification of drugs and medicines by their scientifically and internationally recognize active ingredients or by their official generic name as determined by the Bureau of Food and Drugs of the Department of Health. (2) "Active Ingredient" is the chemical component responsible for the claimed therapeutic effect of the pharmaceutical product. (3)

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