Generic Drug FAQ abc

What is a generic Drug?

A Generic drug is made as soon as the patent of a new

drug has expired. It is the exact same as the original in

virtually everyway.

How are generic drugs regulated?

Generic drugs are regulated by the FDA and must be

tested and authorized by them ahead of production and

afterwards.

Is my generic drug created by the identical organization as the

brand name version? Possibly 50% of all generics are

produced by the business which developed the original drug.

Are Generic drugs produced in the identical common facilities

as brand drugs?

Yes all facilities have to meet FDA requirements.

Why do the branded and generic version of a drug appear

diverse?

Trademark laws do not enable generic versions to look

like other drugs on the market so coloring, size and

shape and so on may possibly be different but they nonetheless act in the

identical way as the difference is in the inactive

ingredients.

What is bioequivalence?

If a generic drug is bioequivalent to the original it

signifies the generic drug functions in precisely the same way.

It releases the identical quantity of the identical active

ingredient in to the blood stream over the identical time

period as the original.

Why are generic drugs less costly?

Due to enhanced competition between pharmaceutical

companies when a patent has been lifted on a

particular drug.

Exactly where are generic drugs developed?

50% of all generic drugs continue to be created by

the firm, which held the original though at a lower

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