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Cimetidine drug manufactured under the brand name Tagamet is used as
a histamine H2-receptor antagonist that inhibits the production of
acid in the stomach. Food and Drug Administration of United states
(US) have certified Tagamet in 1979 to manufacture and market the
drug all over the country. The FDA has made strict specific laws for
the drugs only to be supplied to doctors. FDA also suggests the use
of drugs only to patients suffering from prescribed disease.
Tagamet manufacturer is the sole developer of all types of
Cimetidine drugs in America. Cimetidine pills are marketed by
GlaxoSmithKline under the brand Tagamet. The chemical has to be
clearly mentioned for its certification along with all other
research and clinical trail data’s. FDA provides notices to the
Company relating to ban on sales of drugs to unauthorized sectors,
private marketing, personal gains etc. The strict impositions are to
avoid abuse of such high quality drugs in the community proving safe
application.
In America the product is saled only by Tagamet; any alteration in
the agreement will be treated as an abuse. By excess usage the drug
could be used as a medium of steroid which leads to an out of
control person. FDA thoroughly checks, verifies chemical data,
formula, bioavailability, half-life period, metabolism rate. FDA
states the treatment with the drug is only legalized with the
presence or acceptance of the doctor. Thus the treatment with
Tagamet in the near future can be considered as the best.
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