Facts About Generic Drugs
What is a generic drug?
A generic drug is made one the patent of a new drug has expired. It is the same as the original in just about every way.
How are generic drugs regulated?
Generic drugs are regulated by the FDA and must be tested and then approved by them before it goes into production.
Are your generic drugs made by the same company as the brand name version? It just may be about 50% of all generic drugs are made by the company that developed the original drug.
Are generic drugs made in the same standard facilities as the name brand ones?
Yes al facilities have to meet the FDA standards.
Why do all the brand name and generic drugs look different?
The trademark laws do not allow the generic versions to look just like the originals that are on the market. The coloring, size and shape might be different but they are still going to act the same way and do the same thing.
What is bioequivalaence?
If a generic drug is bioequivalent to the original it may mean that the generic drugs will work in the exact same way. It will release the same amount of the active ingredient in to the blood stream over the same amount of time.
Why are generic drugs so much cheaper?
Because of the increased competition between the pharmaceutical companies once a patent has been lifted on a patent has been lifted on a certain drug they will be cheaper in price.
Why are generic drugs made?
The same company produces Fifty percent of all the generic drugs. Some are made by the developing countries in cases where the drug is exempt in the country from an existing patent in the West.
Generic Drugs
The Regulations Of Generic Drugs
How Pharmaceutical Companies Stop Generics Being Made?
Is There A Difference Between Generic And The Name Brand Drug?
Why Is Generic Drugs Less Expensive?
Generic Drugs
... them. This will require a market that is big enough to attract large amounts of competition that will help to lower the prices. There are some claims that the large Pharmaceutical companies are stopping efforts by countries like India to produce cheaper generic versions of their own drugs. Drugs that ...
The Regulations Of Generic Drugs
... do. Bioequivalence is stated by the FDA to be the absence of a big difference in the rate and extent to how the active ingredient or active moiety in pharmaceutical equivalents or pharmaceutical alternatives are available at the place of the drug action when it is given at the same molar dose under the ...
... period. They cannot patent the active ingredient for more than the length of the paten or renew the paten that has already expired. They can however patent the inactive ingredients and different forms of compounds that are used. Companies can protect their product by patenting the drug like the shape, ...
... that also produce the name brand ones produce Fifty percent of generic drugs. Generic drugs look different to the name brand because the look of the name brand pill is often going to be patented. This means that the generic version ahs to look different in some way but the active ingredients are always ...
... that you have especially if you get worse, you need to go to your GP and get some advice. The research on drugs that you find out about has been well thought out. Researchers do their job and make sure that drugs are safe for the public to use first. Information about generic drugs will allow you to make ...