Generic Drug FAQ
What is a generic Drug?
A Generic drug is created after the patent of a new
drug has expired. It is the same as the original in
How are generic drugs regulated?
Generic drugs are regulated by the FDA and should be
tested and approved by them prior to production and
Is my generic drug made by the same organization as the
brand name version? Possibly 50% of all generics are
made by the business which created the original drug.
Are Generic drugs created in the exact same standard facilities
as brand drugs?
Yes all facilities must meet FDA standards.
Why do the branded and generic version of a drug appear
Trademark laws do not allow generic versions to look
like other drugs on the industry so coloring, size and
shape and so forth may possibly be different but they nonetheless act in the
identical way as the difference is in the inactive
What is bioequivalence?
If a generic drug is bioequivalent to the original it
means the generic drug performs in specifically the identical way.
It releases the identical amount of the very same active
ingredient in to the blood stream over the same time
period as the original.
Why are generic drugs more affordable?
Due to elevated competitors among pharmaceutical
companies when a patent has been lifted on a
Where are generic drugs created?
50% of all generic drugs continue to be developed by
the organization, which held the original though at a lower
cost due to competition. Identify more on our related paper - Hit this webpage: fundable competition
. Some are produced by developing
countries typically in instances where a drug is exempt in
that nation from an existing patent in the West.. Get extra info on a related site - Click here: fundable ledified
. Dig up further on a related website - Visit this URL: ledified fundable