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The 10 most important questions you need to answer before choosing a generic drug versus a
brand name one.
- What are generic drugs?
A generic drug is a copy that is the same as a brand-name drug in dosage, safety,
strength, how it is taken, quality, performance and intended use.
- Are generic drugs as safe as brand-name drugs?
Yes. FDA requires that all drugs be safe and effective. Since generics use the same
active ingredients and are shown to work the same way in the body, they have the same
risks and benefits as their brand-name counterparts.
- Are generic drugs as strong as brand-name drugs?
Yes. FDA requires generic drugs to have the same quality, strength, purity and stability as brand-name drugs.
- Do generic drugs take longer to work in the body?
No. Generic drugs work in the same way and in the same amount of time as brand-name drugs.
- Why are generic drugs less expensive?
Generic drugs are less expensive because generic manufacturers don't have the investment
costs of the developer of a new drug. New drugs are developed under patent protection.
The patent protects the investment - including research, development, marketing, and
promotion - by giving the company the sole right to sell the drug while it is in effect.
As patents near expiration, manufacturers can apply to the FDA to sell generic versions.
Because those manufacturers don't have the same development costs, they can sell their
product at substantial discounts. Also, once generic drugs are approved, there is
greater competition, which keeps the price down. Today, almost half of all
prescriptions are filled with generic drugs.
- Are brand-name drugs made in more modern facilities than generic drugs?
No. Both brand-name and generic drug facilities must meet the same standards of
good manufacturing practices. FDA won't permit drugs to be made in substandard
facilities. FDA conducts about 3,500 inspections a year to ensure standards are met.
Generic firms have facilities comparable to those of brand-name firms. In fact, brand-name
firms are linked to an estimated 50 percent of generic drug production. They frequently
make copies of their own or other brand-name drugs but sell them without the brand name.
- If brand-name drugs and generic drugs have the same active ingredients, why do they look different?
In the United States, trademark laws do not allow a generic drug to look exactly like the brand-name drug.
However, a generic drug must duplicate the active ingredient. Colors, flavors, and certain
other inactive ingredients may be different.
- Does every brand-name drug have a generic counterpart?
No. Brand-name drugs are generally given patent protection for 20 years from the date
of submission of the patent. This provides protection for the innovator who laid out
the initial costs (including research, development, and marketing expenses) to develop
the new drug. However, when the patent expires, other drug companies can introduce competitive
generic versions, but only after they have been thoroughly tested by the manufacturer and
approved by the FDA.
- What is the best source of information about generic drugs?
Contact your physician, pharmacist, or insurance company for information on your generic
drugs. You can also visit the FDA website
for more information.
- What is Generic Initiative for Value and Efficiency (GIVE)?
On October 4, 2007, FDA launched the Generic Initiative for Value and Efficiency,
or GIVE. The initiative will use existing resources to help FDA modernize and
streamline the generic drug approval process.
Source: FDA/Center for Drug Evaluation and Research Date created: July 31, 2002; Last updated: October 4, 2007
Adapted by Editorial Staff, December 2007
Last update, August 2008