
The Federal Drug Administration imposes a time limit on the
patent. The length of time one remains in outcome varies from country to
country. Once the patent has expired, other manufacturers are entitled to create
a generic version of the drug.
The generic must contain the active ingredients the unique
brand name drug has. The FDA needs this. The generic edition must be almost equal
to the brand name (the active ingredients must be nearly the same).
The cost of generic drugs is much lesser than the brand name
for two superior reasons. They are copied, which relieves them of the cost of
research and medical trials. Another cause is that more than one company can
manufacture a generic edition.
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