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generic name Definitions

noun

the name given to a drug that is used to identify it irrespective of trademark etc.

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  • generic drugs tend to be priced lower than their brand-name counterparts. when enrollees choose a generic over a brand-name drug to fill a prescription, the plan sponsor accrues substantial savings; therefore, many plans offer more generous coverage for generic substitutes. the percentage of employees in plans that offer this type of cost saving incentive has increased markedly over the past decade, to 83 percent in 2003. bls.gov

  • in the united states, there are four fda-approved antiviral drugs recommended by cdc this season. three are neuraminidase inhibitor antiviral drugs: oseltamivir (available as a generic version or under the trade name tamiflu®) for oral administration, zanamivir (trade name relenza®) for oral inhalation using an inhaler device, and peramivir (trade name rapivab®) for intravenous administration. the fourth is a cap-dependent endonuclease (cen) inhibitor, baloxavir marboxil (trade name xofluza®) for oral administration, approved for use in the united states during the 2018-2019 season by fda in october of 2018. cdc.gov

  • a third limitation in taxpayer reporting is that the "city name" reported in question a was not always the name of an actual city (or town). often, because the name reported in this item was a post office name, procedures needed to be implemented to account for these. the coding materials were designed to contain post office names as well as actual city (or town) names, thus, it was possible to assign grin codes to these names. census.gov

  • this new edition of the book adds five new techniques, plus a discussion of “intuitive versus analytic approaches to thinking.” (xviii) there are also stimulating inputs on dealing with cognitive bias, idea generation, and challenge analysis to name just a few. while the emphasis is on intelligence analysis, they point out that the structured techniques described are generic in applicability and can be used in any situation—police, security, corporate conflict management—where one is tasked with sorting out often conflicting and incomplete data. cia.gov

  • epocrates provides monographs based on product-specific information, such as available formulations, dosing, indications, manufacturer, and pricing. for example, epocrates includes a unique monograph for each brand name albuterol inhaled product (i.e., proair hfa, proair respiclick, proventil hfa, ventolin hfa), as well as a generic albuterol inhaled monograph. the generic monograph covers only the strengths and forms available on the us market as generic products. the brand name monographs are specific to each brand product. epocrates.com

  • the first scam is the brand name scam. aleve is the brand name for naproxen; advil for ibuprofen; and tylenol for acetaminophen. why anyone would pay for the brand name product when the shelves adjacent to them contain the equally effective generic product for a fraction of the price is beyond me. and your pharmacy makes it easy for you to find the generic product. it's right next to the brand name one! just look for the generic name: naproxen, ibuprofen or acetaminophen. all the major chain pharmacies have their own line of generic products; many even have little signs that say “compare to brand name x.” and all you need to compare is the price. everydayhealth.com

  • there are generic versions of both over-the-counter and prescription medications, but not all drugs have generic equivalents. generic drugs can only be produced when a patent on a brand name drug expires or when a patent has never existed. they are generally cheaper than the equivalent brand name drug because of much lower marketing and development costs. because a generic competitor can hurt a brand name manufacturer's profits, drug companies have used legal action and regulatory delays to slow the introduction of generics, or have paid generic manufacturers to postpone the production and marketing of generics. the medicare overhaul legislation passed in 2003 contained sections designed to speed the introduction of generic drugs by making it easier to challenge weak or invalid drug patents. production of generic drugs (and increasingly, drug generally) in foreign countries, however, has been hard for the food and drug administration inspect and certify. factmonster.com

  • statins work by blocking hmg-coa reductase. that’s an enzyme your liver uses to make cholesterol. statins also help your body reabsorb built-up cholesterol deposits from your arteries. most people can take statins without difficulty, but some people can’t tolerate side effects like digestive problems and muscle pain. statins have been around for a long time, so your doctor can give you information about how they work in the long term. they’re available in brand name and generic tablets and have become quite affordable. healthline.com

  • not surprisingly, the marketing techniques of brand name and generic manufacturers differ considerably. brand name manufacturers tend to focus their marketing strategies primarily on physicians, who will potentially prescribe their products, while the generic manufacturers focus on the purchasers, e.g. pharmacies and hospitals. since generic drugs tend to be less expensive than brand name drugs, they are as a rule preferred by insurance programs and other third-party payers and even required when available for reimbursement. there are exceptions to this rule, however, such as when a large purchaser may negotiate a brand name price that is competitive if not less expensive than the generic alternative. hhs.gov

  • there are generic versions of both over-the-counter and prescription medications, but not all drugs have generic equivalents. generic drugs can only be produced when a patent on a brand name drug expires or when a patent has never existed. they are generally cheaper than the equivalent brand name drug because of much lower marketing and development costs. because a generic competitor can hurt a brand name manufacturer's profits, drug companies have used legal action and regulatory delays to slow the introduction of generics, or have paid generic manufacturers to postpone the production and marketing of generics. the medicare overhaul legislation passed in 2003 contained sections designed to speed the introduction of generic drugs by making it easier to challenge weak or invalid drug patents. production of generic drugs (and increasingly, drug generally) in foreign countries, however, has been hard for the food and drug administration inspect and certify. infoplease.com

  • - for personal names, type last name first name: hillerman tony - for corporate names, type in order: sony music entertainment; walt disney company for claimant names, go to other search options and select "name: claimant (klcn)" from the search by box. for personal names, type first name last name: james michener. for corporate names, type in order: metro goldwyn mayer for document names, go to other search options and select either "docs: party1 statement (k291)" or "docs: party2 (k292)", or "docs party1/2 (kpty)" from the search by box. for personal names, type first name last name: stephen king. for corporate names, type in order: warner brother pictures loc.gov

  • breanne's physician explained that the multifaceted pain rehabilitation program at mayo clinic would open soon, and it had the potential to change a person's life. when asked if she would like her name put on a list for the new program, breanne's answer was immediate. "i was like, 'double-star my name!'" she says. mayoclinic.org

  • in most instances, generic drugs work as well as the brand name drugs. unless your health care practitioner advises against the use of the generic product, it will be less expensive to use the generic product. all too often, individuals purchase the more expensive brand name drug because they believe that the generic equivalent is inferior. in most states, as long as the prescriber does not indicate otherwise, pharmacists are required by law to substitute generic products for brand name products. medicinenet.com

  • generic drugs are copies of brand name drugs. they have the same exact medicine as a brand name drug. a generic is approved as safe and effective by the food and drug administration (fda). the brand name drug costs more because of the research that went into making it. the generic drug is the same drug, and it costs less money. medlineplus.gov

  • "before the introduction of the generic drug, the maker of the brand name drug worked to push its market share from the 20 mg dose to the 40 mg dose, which was not interchangeable with the new generic," hartung said. "the low market share for the generic drug was also because the generic drug was only 15% less expensive than the brand name drug at 20 mg at approximately the same cost as the 40 mg dose when it launched," he added. medpagetoday.com

  • 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 but can create their own brand name. as a result, the same generic drug may be sold under either the generic name (for example, ibuprofen) or one of many brand names (such as advil or motrin). merckmanuals.com