![]() By law, generic drugs must have the same active ingredients as the brand name product, and they can be expected to have the same effect when used in place of a brand name drug. However, generic drugs still must meet strict FDA requirements with respect to quality, performance, labeling, manufacturing, and bioequivalence. Generic drugs have lower research costs and increased market competition and those substantial savings are passed on to the patient. ![]() When the patent expires, other manufacturers can submit an abbreviated new drug application (ANDA) to the FDA for approval to market the generic version. During this period of patent protection, only the original manufacturer can research, develop and sell the brand name drug. Patents typically expire 20 years from the date of filing. A drug manufacturer applies for a patent to protect their drug from being copied and sold by another company and losing profits. For example, generic fluoxetine could not be sold until the patent had expired on the brand name equivalent Prozac. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Generics cannot be sold until after the drug patent expires on the original brand name product. Food and Drug Administration, and are deemed to be as safe and effective as the brand name product. A generic drug must have the same active ingredients, route of administration, dosage form, strength, and indications as the original brand product. Ask your health care provider for advice if you are unsure about the online purchase of any medication.Ī generic drug is equivalent to its brand name counterpart, but is usually much less expensive. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. These medications may be counterfeit and potentially unsafe. Fraudulent online pharmacies may attempt to sell illegal "generic" versions of these brand name medications. Web page provides quick links to everything from acronyms to wholesale distributor and third-party logistics. Food and Drug Administration and may be covered by legal patents that delay the availability of lower cost generic substitutes. Additional topics include: approved REMS, drug shortages, and the Orange book. Always consult your healthcare provider before changing any medicines.īrand name prescription medications are approved by the U.S. Note: Generic drug information listed on the website should be used as a guideline only.
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