FACT: FDA require generic drugs to have the same quality and performance as brand name drugs.
When a generic medicine product is approved, it has metexact standards established by the FDA with respect toidentity, strength, quality, purity, and potency. However,some variability can and does occur during manufacturing,for both brand name and generic drugs. When a drug,generic or brand name, is mass-produced, very smallvariations in purity, size, strength, and other parameters arepermitted. FDA limits how much variability is acceptable.
Generic drugs are required to have the identical active ingredient, strength, dosage form, and route of administration as the brand name product. Generic drugs do not need to contain the same inactive ingredients as the brand name product. The generic drug manufacturer must prove its drug is the same as (bioequivalent) the brand name drug. For example, after the patient takes the generic drug, the amount of drug in the bloodstream is measured. If the levels of the drug in the bloodstream are the same as the levels found when the brand name product is used, the generic drug will work the same.
Through review of bioequivalence data, FDA ensures that the generic product performs the same as its respective brand name product. This standard applies to all generic drugs, whether immediate or controlled release.
All generic manufacturing, packaging, and testing sites must pass the same quality standards as those of brand name drugs, and the generic products must meet the same exacting specifications as any brand name product. In fact, many generic drugs are made in the same manufacturing plants as brand name drug products.
FACT: Research shows that generics work just as well as brand name drugs.
A study evaluated the results of 38 published clinical trials that compared cardiovascular generic drugs to their brand name counterparts. There was no evidencethat brand name heart drugs worked any better than generic heart drugs.
FACT: FDA does not allow a 45 percent difference in the effectiveness of the generic drug product.
FDA recently evaluated 2,070 human studies conductedbetween 1996 and 2007. These studies compared theabsorption of brand name and generic drugs into a person’sbody. These studies were submitted to FDA to supportapproval of generics. The average difference in absorptioninto the body between the generic and the brand name was3.5 percent. Some generics were absorbed slightly more,some slightly less. This amount of difference would beexpected and acceptable, whether for one batch of brandname drug tested against another batch of the same brand,or for a generic tested against a brand name drug. In fact, there have been studies in which brand name drugs were compared with themselves as well as with a generic. As a rule, the difference for the generic-to-brand comparison was about the same as the brand-to-brand comparison.
Any generic drug modeled after a single, brand name drug must perform approximately the same in the body as the brand name drug. There will always be a slight, but not medically important, level of natural variability – just as there is for onebatch of brand name drug compared to the next batch of brand name product.
FACT: When it comes to price, there is a big difference between generic and brand name drugs. On average, the cost of a generic drug is 80 to 85 percent lower than the brand name product.
In 2010 alone, the use of FDA-approved generics saved $158 billion, an average of $3billion every week.
FACT: Cheaper does not mean lower quality.
Generic manufacturers are able to sell their products for lower prices because they arenot required to repeat the costly clinical trials of new drugs and generally do not pay for costly advertising, marketing, and promotion. In addition, multiple generic companies are often approved to market a single product; this creates competition in the market place, often resulting in lower prices.
FACT: FDA monitors adverse events reports for generic drugs.
The monitoring of adverse events for all drug products,including generic drugs, is one aspect of the overall FDAeffort to evaluate the safety of drugs after approval. Manytimes, reports of adverse events describe a known reaction tothe active drug ingredient.
Reports are monitored and investigated, when appropriate. The investigations may lead to changes in how a product (brand name and generic counterparts) is used or manufactured.
FACT: FDA is actively engaged in making all regulated products – including generic drugs – safer.
FDA is aware that there are reports noting that some people may experience an undesired effect when switching from brand name drug to a generic formulation or from one generic drug to another generic drug. FDA wants to understand what may cause problems with certain formulations if, in fact, they are linked to specific generic products.
FDA is encouraging the generic industry to investigate whether, and under what circumstances, such problems occur. The Agency does not have the resources to perform independent clinical studies and lacks the regulatory authority to require industry to conduct such studies. FDA will continue to investigate these reports to ensure that it has all the facts about these treatment failures and will make recommendations to healthcare professionals and the public if the need arises.
 Kesselheim et al. Clinical equivalence of generic and brand name drugs used in cardiovascular disease: a systematic review and meta-analysis. JAMA. 2008;300(21)2514- 2526
 Davit et al. Comparing generic and innovator drugs: a review of 12 years of bioequivalence data from the United States Food and Drug Administration. Ann Pharmacother. 2009;43(10):1583-97.
 SAVINGS An Economic Analysis of Generic Drug Usage in the U.S., GPhA, September 2011, page 1.