Republic Act of 1988 – Generics Act of 1988 Flashcards
not covered by patent protection and which are
labeled solely by their international non-proprietary or generic name
generic drugs
propriety name given by the manufacturer to
distinguish its product from those of competitors
brand name
a list of alternative drugs used when there is no
response to the core essential drug
complementary list
list of drugs that meets the health care needs of the majority of the population
core list
“National Drug Formulary” is a list of drugs
prepared and periodically updated by the Department of Health
essential drugs list
consist of a core list and a complementary list
essential drug lists
drugstore, pharmacies, and any other business
establishments which sell drugs or medicines
drug outlets
organization or company involved in the
manufacture, importation, repacking and/or distribution of drugs or medicines
drug establishment
finished product form that contains the active
ingredients
drug product
description of the chemical structure of the drug or medicine and serves as the complete identification of a compound
chemical name
chemical component responsible for the claimed therapeutic effect of the pharmaceutical product
active ingredient
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
generic name of generic terminology
Generics Act of 1988
Republic Act 6675