Are generic drugs the same as name brand drugs?

Generic drugs are exactly the same as name brand drugs in every pharmacological sense: effectiveness, strength, dosage amount, etc. The only difference is that generic drugs are cheaper because the manufactures of the generic drugs do not have to pay the costs associated with marketing their items. For proof, the FDA regulates the effectiveness of generic drugs. You can also check out this website: medicinenet.com/script/main/art.asp?arti....

I know for a fact that some generic drugs do not work the same as the name brand products. The active ingredients are the same in name brand and generic drugs. However, the inactive ingredients are not.

Just because the inactive ingredients are not "active", doesn't mean that it will increase or decrease the drugs performance. Even different generics can work differently. I took two different types of generic Wellbutrin.

These were exactly the same dosage, the pills where made different. One was stronger than the other. Some people tried to tell me this was in my head, but after long research.

I seen many others had complained about the same brand. Then after a great deal of other related research, I found out why. The filler of the medications were different.My grandmother and mother have also been victims of the generic drugs not carry out it's duties like the name brand.

In fact, my grandmothers doctor would have to specify on one of her pills that it had to be the name brand. The generic didn't even work for her, and nearly killed her because it was heart medication. Are the active ingredients the same?

Yes Are the fillers the same? No Are the dyes the same? No Are they equal?

No These inactive ingredients contain different chemicals. I am including a ton of sources to back up my claim.

There are eight major parts to the FDA's review of a firm's application to sell a generic drug: * There must be an FDA-approved brand-name drug that is the reference for the proposed generic. The generic must have the same active ingredient or ingredients and the same labeled strength as this reference product. It must have the same dosage form-tablets, patches and liquids are examples of dosage forms.It must be administered the same way, for example, swallowed as a pill or given as an injection.

* The manufacturer must show the generic drug is "bioequivalent" to the brand-name drug. * The generic drug's labeling must be essentially the same as that of the approved drug. * The firm must fully document the generic drug's chemistry, manufacturing steps, and quality control measures.

Each step of the process must be detailed for FDA review. * The firm must assure the FDA that the raw materials and the finished product meet USP specifications, if these have been set. The USP, or U.S. Pharmacopoeia, is the non-profit, scientific body chartered by Congress to set standards for drug purity in this country.

* The firm must show that its generic drug maintains stability as labeled before it can be sold. Once on the market, the firm must continue to monitor the drug's stability. The firm must show that the container and its closure system won't interact with the drug.

Firms making sterile drugs must submit sterility assurance data showing microbiologic integrity of these products. * The firm must provide a full description of the facilities it uses to manufacture, process, test, package, label and control the drug.It must certify that it complies with federal regulations about current good manufacturing practices and undergo FDA inspection of the manufacturing facility to assure compliance. * Before FDA approves a generic drug, it usually conducts an inspection at the proposed manufacturing site to make sure the firm is capable of meeting its application commitments and to ensure the firm can manufacture the product consistently.

Sources: fda.gov/Drugs/EmergencyPreparedness/Biot... http://www.originaldrugs.com/blog/general/brand-vs-generic-drugs.

Yes, generic drugs are the same as brand name drugs in their formulation, active ingredient, dosage, intended use, effects, side effects, risks, safety, and strength. Basically, that is saying they are exactly the same as the name brand drugs. There are myths that generic drugs are inferior in quality to brand name drugs.

This is absolutely not true as the FDA applies the same standards for all drug manufacturers. The FDA estimates that half of generic drug production is by brand name companies. People wonder why the generic drugs are so much cheaper than the equivalent brand name drug.

That's basically because manufacturers haven't had time to market the drug. When a new drug comes onto the market, there has already been a lot of money spent on the drug with research and marketing. A patent is granted and when the patent is about to expire, the companies can get permission from the FDA to make a generic form of the drug which they can sell cheaper.

The only difference in the generic drug is shape and color since they are not allowed by United States trademark laws to look exactly like the name brand drug. Another common misbelief is that generic drugs take longer to work. The FDA requires that generic drugs work as fast and as effectively as the original brand-name products.

Yes, generic drugs and brand name drugs are exactly the same. They have the same dosage, intended use, effects, side effects, route of administration, risks, safety and strength as the original drug. So it would follow then that the pharmacological effects are exactly the same as those with their branded counterparts.

However, many people are concerned that since generic are cheaper, they thought that the quality and effectiveness will be compromised to make the cheap generic drug. But the FDA requires that all generic drugs be safe and effective to use as the branded drugs. Generic drugs are cheaper because manufacturers did not have any expenses in developing and marketing a new drug.

When a certain company introduces a new drug into the market, the firm has already spent a lot of money on research, development, marketing, and promotion of the certain drug. A patent is then granted so that the company will be able to developed the drug and have its exclusive rights to sell the drug as long as the patent is in effect. If the patent nearly expire, manufacturers can apply to the FDA for permission to make and sell generic versions of the drug.So they were able to save because there is no start up cost for the research and development of the drug and so companies can afford to make and sell it at a cheaper price.

This is the reason why generic drugs are cheaper. Competition between companies can also lower the price.So, there is no truth that generic drugs are manufactured in a poor quality facilities and that they are inferior in quality to brand-name drugs. FDA applies the same standards for all drug manufacturing facilities.

There are several companies that manufacture both brand names and generic drugs. FDA estimated that 50% of generic drug that are produced by brand-name companies. It is also untrue that generic drug takes longer time to work since FDA requires that generic drugs work as fast and as effectively as the original bran-name products.

There are generic versions that have different colors, flavors or combination of inactive ingredients than original because trademark law in the U.S.Prohibit the generic drugs to look exactly like the brand-name ones. But the active ingredients are exactly the same in both preparations to ensure that both have the same effectiveness and medicinal benefits.

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