Generic Drug Production
Before a company can make a generic drug, its bioequivalent brand-name counterpart must have been created, approved and distributed. While a pharmaceutical company is making a new brand-name drug, a patent ensures that company may develop, manufacture and sell the drug for a certain amount of time. Patent time frames vary, and in most situations, a patent cannot be renewed after it expires. In the United States, an average drug patent lasts for 17 years.
![]() Chad Baker/Ryan McVay/Photodisc/Getty Images Once the patent for a brand-name drug expires, other companies can produce generic versions. |
Once the patent expires, other companies can produce generic versions. To start the process, drug manufacturers file an Abbreviated New Drug Application (ANDA) with the FDA. But before the FDA approves the application, the generic drug must meet the same standards that the original brand-name drug met. According to the Drug Price Competition and Patent Term Restoration Act of 1984 (the Hatch-Waxman Act), bioequivalence is the main basis for approval of generic drugs. The generic drug must contain the same active ingredients, have identical strength and form and have a similar route of administration as the brand-name drug. The generic drug must also be used for the same ailments that the brand-name drug is used.
For more information on generic drugs, check out the links on the next page.


