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Generic Drug FAQ


What is a generic Drug?

A Generic drug is developed once 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 have to be

tested and approved by them before production and

afterwards.

Is my generic drug produced by the same firm as the

brand name version? Possibly 50% of all generics are

made by the company which developed the original drug.

Are Generic drugs made in the identical common facilities

as brand drugs?

Yes all facilities have to meet FDA standards.

Why do the branded and generic version of a drug look

diverse?

Trademark laws do not enable generic versions to appear

like other drugs on the industry so coloring, size and

shape and so forth may possibly be diverse but they nevertheless act in the

same way as the difference is in the inactive

ingredients.

What is bioequivalence?

If a generic drug is bioequivalent to the original it

implies the generic drug performs in specifically the identical way.

It releases the very same quantity of the same active

ingredient in to the blood stream over the very same time

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Why are generic drugs less costly?

Due to improved competitors amongst pharmaceutical

businesses when a patent has been lifted on a

distinct drug.

Exactly where are generic drugs created?

50% of all generic drugs continue to be created by

the firm, which held the original although at a lower

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