Crossword Solver > found answer > GENERICDRUG (generic drug)

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genericdrug

generic drug

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The answer GENERICDRUG (generic drug) has 0 possible clue(s) in existing crosswords.

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The word GENERICDRUG (generic drug) is NOT valid in any word game. (Sorry, you cannot play GENERICDRUG (generic drug) in Scrabble, Words With Friends etc)

There are 11 letters in GENERICDRUG ( C³D²E¹G²I¹N¹R¹U¹ )

To search all scrabble anagrams of GENERICDRUG, to go: GENERICDRUG?

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8 letters out of GENERICDRUG

DERINGER DREGGIER DRUGGIER GINGERED GRUNGIER INCURRED RECEDING REDUCING REINDUCE RENIGGED RERIGGED RUGGEDER UNRIGGED

7 letters out of GENERICDRUG

6 letters out of GENERICDRUG

5 letters out of GENERICDRUG

4 letters out of GENERICDRUG

3 letters out of GENERICDRUG

CEE CIG CRU CUD CUE CUR DEE DEN DIE DIG DIN DUE DUG DUI DUN ECU EGG END ENG ERE ERG ERN ERR GED GEE GEN GID GIE GIG GIN GNU GUN ICE IGG IRE NEE NEG REC RED REE REG REI RID RIG RIN RUE RUG RUN URD URN

2 letters out of GENERICDRUG

DE ED EN ER ID IN NE NU RE UN

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Definitions of generic drug in various dictionaries:

noun - when the patent protection for a brand-name drug expires generic versions of the drug can be offered for sale if the FDA agrees

GENERIC DRUG - A generic drug is a pharmaceutical drug that has the same chemical substance as the drug that was originally developed, patented and innovated. Gener...

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Last Seen in these Crosswords & Puzzles
Dec 17 2017 The Times - Specialist

Generic drug description
A generic drug is a pharmaceutical drug that has the same chemical substance as the drug that was originally developed, patented and innovated. Generic drugs are allowed for sale after the expiry of the patent of the original drugs. Because the active chemical substance is the same, the medical profile of generics is believed to be equivalent in performance. The generic drug has the same Active Pharmaceutical Ingredient (API) as the original, but it may differ in characteristics such as manufacturing process, formulation, excipients, color, taste, and packaging.Although they may not be associated with a particular company, generic drugs are usually subject to government regulations in the countries in which they are dispensed. They are labeled with the name of the manufacturer and a generic non-proprietary name such as the United States Adopted Name or international non-proprietary name of the drug. A generic drug must contain the same active ingredients as the original brandname formulation. The U.S. Food and Drug Administration (FDA) requires generics to be identical to or within an acceptable bioequivalent range of their brandname counterparts, with respect to pharmacokinetic and pharmacodynamic properties. (The FDA's use of the word "identical" is a legal interpretation, not literal.) * Biopharmaceuticals, such as monoclonal antibodies, differ biologically from small molecule drugs. Biosimilars have active pharmaceutical ingredients that are almost identical to the original product and are typically regulated under an extended set of rules, but they are not the same since generic drugs as the active ingredients are not the same as those of their reference products.In most cases, generic products become available after the patent protections, afforded to a drug's original developer, expire. Once generic drugs enter the market, competition often leads to substantially lower prices for both the original brandname product and its generic equivalents. In most countries, patents give 20 years of protection. However, many countries and regions, such as the European Union and the United States, may grant up to five years of additional protection ("patent term restoration") if manufacturers meet specific goals, such as conducting clinical trials for pediatric patients.Manufacturers, wholesalers, insurers, and drugstores can all increase prices at various stages of production and distribution.In 2014, according to an analysis by the Generic Pharmaceutical Association, generic drugs accounted for 88% of the 4.3 billion prescriptions filled in the United States."Branded generics" on the other hand are defined by the FDA and NHS as "products that are (a) either novel dosage forms of off-patent products produced by a manufacturer that is not the originator of the molecule, or (b) a molecule copy of an off-patent product with a trade name." Since the company making branded generics can spend little on research and development, it is able to spend on...

Generic drug description

A generic drug is a pharmaceutical drug that has the same chemical substance as the drug that was originally developed, patented and innovated. Generic drugs are allowed for sale after the expiry of the patent of the original drugs. Because the active chemical substance is the same, the medical profile of generics is believed to be equivalent in performance. The generic drug has the same Active Pharmaceutical Ingredient (API) as the original, but it may differ in characteristics such as manufacturing process, formulation, excipients, color, taste, and packaging.Although they may not be associated with a particular company, generic drugs are usually subject to government regulations in the countries in which they are dispensed. They are labeled with the name of the manufacturer and a generic non-proprietary name such as the United States Adopted Name or international non-proprietary name of the drug. A generic drug must contain the same active ingredients as the original brandname formulation. The U.S. Food and Drug Administration (FDA) requires generics to be identical to or within an acceptable bioequivalent range of their brandname counterparts, with respect to pharmacokinetic and pharmacodynamic properties. (The FDA's use of the word "identical" is a legal interpretation, not literal.)
* Biopharmaceuticals, such as monoclonal antibodies, differ biologically from small molecule drugs. Biosimilars have active pharmaceutical ingredients that are almost identical to the original product and are typically regulated under an extended set of rules, but they are not the same since generic drugs as the active ingredients are not the same as those of their reference products.In most cases, generic products become available after the patent protections, afforded to a drug's original developer, expire. Once generic drugs enter the market, competition often leads to substantially lower prices for both the original brandname product and its generic equivalents. In most countries, patents give 20 years of protection. However, many countries and regions, such as the European Union and the United States, may grant up to five years of additional protection ("patent term restoration") if manufacturers meet specific goals, such as conducting clinical trials for pediatric patients.Manufacturers, wholesalers, insurers, and drugstores can all increase prices at various stages of production and distribution.In 2014, according to an analysis by the Generic Pharmaceutical Association, generic drugs accounted for 88% of the 4.3 billion prescriptions filled in the United States."Branded generics" on the other hand are defined by the FDA and NHS as "products that are (a) either novel dosage forms of off-patent products produced by a manufacturer that is not the originator of the molecule, or (b) a molecule copy of an off-patent product with a trade name." Since the company making branded generics can spend little on research and development, it is able to spend on...

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