How do I find my authorized generics?
See if your medication has an authorized generic. The data behind your search results has been sourced from the U. S. Food and Drug Administration website (https://www.fda.gov/drugs).
What is generic name with example?
For example, phenytoin is the generic name and Dilantin is a brand name for the same drug, which is a commonly used antiseizure drug. The generic name is assigned, in the United States, by an official body—the United States Adopted Names (USAN) Council.
How do you identify generic name and brand name?
The brand name is usually written most clearly on any packaging. However, you will always see the generic name written somewhere on the packet (often in small print). Some medicines only have the generic name on the packet.Oct 16, 2017
Do all drugs have a generic name?
Do all brand-name drugs have a generic equivalent? NO. Generic drugs usually become available after patents protecting a brand-name medicine expire.Jun 25, 2019
What is generic drug?
What are generic drugs? A generic drug is a medication created to be the same as an already marketed brand-name drug in dosage form, safety, strength, route of administration, quality, performance characteristics, and intended use.
What is the label for generic medicine?
The container in which the medicine will be shipped and sold is appropriate. The label is the same as the brand-name medicine's label. The drug information label for the generic medicine should be the same as the brand-name label.
Why do FDA inspectors go to the generic drug manufacturer's facility?
FDA scientists review those procedures, and FDA inspectors go to the generic drug manufacturer's facility to verify that the manufacturer is capable of making the medicine consistently and to check that the information the manufacturer has submitted to FDA is accurate.
What is the FDA's drug program?
The FDA Generic Drugs Program conducts a rigorous review to ensure generic medicines meet these standards, in addition to conducting inspections of manufacturing plants and monitoring drug safety after the generic medicine has been approved and brought to market.
Why do generic drugs cost less than brand names?
Generic drugs tend to cost less than their brand-name counterparts because generic drug applicants do not have to repeat animal and clinical (human) studies that were required of the brand-name medicines to demonstrate safety and effectiveness.
How much less is generic medicine?
The reduction in upfront research costs means that, although generic medicines have the same therapeutic effect as their branded counterparts, they are typically sold at substantial discounts, an estimated 80 to 85% less, compared with the price of the brand-name medicine.
What is DCAP in drug review?
In 2017, FDA announced the Drug Competition Action Plan (DCAP) to further encourage robust and timely market competition for generic drugs and help bring greater efficiency and transparency to the generic drug review process, without sacrificing the scientific rigor underlying our generic drug program. Back to Top.
What does the prefix "citinib" mean?
Sometimes a substem is used to further classify drugs, such as how “-citinib” denotes drugs that inhibit a specific family of TYK inhibitors, the Janus kinases. A one- or two-syllable prefix. This differentiates each drug from others in its class.
What does stem mean in medicine?
A stem or substem. Usually appearing at the end of the name, this signifies a chemical structure, indication or action at a specific receptor. For example, for the cancer drug imatinib, “-tinib" refers to a drug’s action as a tyrosine kinase (TYK) inhibitor. Sometimes a substem is used to further classify drugs, ...
What are the implications of the USAN Council?
Implications for safety, access. The class to which a drug is assigned can affect a manufacturer’s decisions about whether to continue developing a drug, so the USAN Council must balance pharmaceutical firms’ name preferences with its obligations regarding patient safety and access to drugs.
How is a generic drug assigned?
The generic name is assigned, in the United States, by an official body— the United States Adopted Names (USAN) Council. The brand name is developed by the company requesting approval for the drug and identifies it as the exclusive property of that company. When a drug is under patent protection, the company markets it under its brand name.
What is generic name?
The term generic, when applied to such items as foods and household products, is used to describe a less expensive, sometimes less effective or lower-quality copycat version of a brand-name product .
What happens when a drug is patent protected?
When a drug is under patent protection, the company markets it under its brand name. When the drug is off-patent (no longer protected by patent), the company may market its product under either the generic name or brand name. Other companies that file for approval to market the off-patent drug must use the same generic name ...
Why are generic and brand names unique?
Generic and brand names must be unique to prevent one drug from being mistaken for another when drugs are prescribed and prescriptions are dispensed. To prevent this possible confusion, the FDA must agree to every proposed brand name.
How long does it take for a patent to expire?
Additional patents can sometimes be filed to extend the patent life. Usually, about 10 years elapse between the time a drug is discovered (when the patent is obtained) and the time the drug is approved for human use, leaving the company only about half of the patent time to exclusively market a new drug.
How long do you have to patent a drug?
Thus, a company often owns more than one patent for a drug. Patents grant the company exclusive rights to a drug for 20 years. Additional patents can sometimes be filed to extend the patent life. Usually, about 10 years elapse between the time a drug is discovered (when the patent is obtained) and the time the drug is approved for human use, leaving the company only about half of the patent time to exclusively market a new drug. The Food and Drug Administration (FDA) may choose to accelerate the approval process for drugs to treat acquired immunodeficiency syndrome (AIDS), cancer, and other life-threatening disorders when no current effective treatment exists.
Why do doctors use generic names?
However, doctors often use the brand name on prescriptions, because it is easier to remember and doctors usually learn about new drugs by the brand name. Generic names are usually more complicated and harder to remember than brand names. Many generic names are a shorthand version of the drug’s chemical name, structure, or formula.
What is generic drug?
A generic drug is equivalent to its brand name counterpart, but is usually much less expensive. A generic drug must have the same active ingredients, route of administration, dosage form, strength, and indications as the original brand product.
When can generic drugs be sold?
Generics cannot be sold until after the drug patent expires on the original brand name product.
How long does a patent last?
A drug manufacturer applies for a patent to protect their drug from being copied and sold by another company and losing profits. Patents typically expire 20 years from the date of filing. During this period of patent protection, only the original manufacturer can research, develop and sell the brand name drug.
Do generic drugs have the same ingredients as brand drugs?
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. See also: Generic drugs.
Do generic drugs have to meet FDA requirements?
However, generic drugs still must meet strict FDA requirements with respect to quality, performance, labeling, manufacturing, and bioequivalence.
What is generic medication?
A generic medication, also approved by the FDA, is basically a copy of the brand name drug and is marketed under its chemical name.
What is the difference between generic and brand name drugs?
A brand name drug in the U.S. is approved by the Food and Drug Administration (FDA), and is supplied by one company - the pharmaceutical manufacturer. The drug is protected by a patent and is marketed under the manufacturer's brand name. Whereas a generic medication, also approved by the FDA, is basically a copy of the brand name drug ...
How much money did generic drugs save in 2010?
Generic Drug Facts and Statistics. In 2010 the use of FDA approved generics saved $158 billion, an average of $3 billion every week. The U.S. FDA requires generic drugs have the same high quality, strength, purity and stability as brand-name drugs.
Why are generic drugs cheaper than brand names?
Generic drugs are cheaper than brand name drugs because the manufacturer does not have to spend money to discover and test the drug. Although generic drugs are chemically identical to their branded counterparts, they are typically sold at substantial discounts from the branded price.
How much cheaper is generic than brand?
On average, the cost of a generic drug is 80 to 85 percent lower than the brand name product. Prescriptions may be issued for drugs specifying only the chemical name, rather than a manufacturer's name; such a prescription can be filled with a drug of any brand meeting the specification.
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Disabled World is an independent disability community established in 2004 to provide disability news and information to people with disabilities, seniors, and their family and/or carers. See our homepage for informative reviews, exclusive stories and how-tos.
Do generic drugs have the same quality as brand names?
And, the generic manufacturing, packaging, and testing sites must pass the same quality standards as those of brand name drugs. Approximately half of all brand name drugs on the market have generic versions.
What is the main salt in Crocin?
For instance, if the doctor has prescribed Crocin, a branded drug commonly used to treat fever and pain, the main salt in the drug is Paracetamol. The chemist may thus suggest another drug – branded or unbranded - that has similar amount of Paracetamol.
Does HealthKartPlus confuse consumers?
HealthKartPlus doesn’t confuse consumers with excess jargon - you will learn about the salts in the drug, substitutes offered by other brands and their respective prices. GetDavai.com - This is primarily for comparing drug prices with the same constituents but from different brands.
Is Med India a good site to compare generic drugs?
Med India is not the most user-friendly site (ad-heavy) but it does help you compare the prices of various brands of drugs with the same generic drug. HealthKartPlus.com – This is another generic drug search engine that is also available as an app for Android and iOS devices.
