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NDA
(redirected from New drug application)

   Also found in: Medical, Wikipedia 0.01 sec.
AcronymDefinition
NDANew Drug Application (US FDA)
NDANon-Disclosure Agreement
NDANational Democratic Alliance (group of political parties in India)
NDANotre Dame Academy
NDANational Defence Academy (military training school in India)
NDANational Disability Authority (Ireland)
NDANuclear Decommissioning Authority (UK)
NDANational Defense Academy (Japan)
NDANational Dance Association
NDANational Department of Agriculture (South Africa)
NDANext Day Air
NDANo Data Available
NDANational Dental Association
NDANissan Design America (La Jolla, CA)
NDANevada Development Authority
NDANational Dart Association
NDANational Defence Act (Canada)
NDANational Day of Action
NDANon-Destructive Assay
NDANational Directory Assistance (Sprint)
NDANederlandse Dealer Associatie (Dutch)
NDANational Deaf Academy
NDANon-Data-Aided
NDANever Die Alone
NDANew Defence Agenda (Brussels, Belgium)
NDANon-Destructive Analysis
NDANational Drilling Association
NDANiagara Divers' Association
NDANational Defense Area
NDANon-Disturbance Agreement
NDANational Defense Act (USA)
NDANepal Dental Association (Lalitpur, Nepal)
NDANot Diagnosed with Anything
NDANetwork Data Anonymization
NDANo Detectable Activity
NDANorthern Domestic Airspace
NDANight Duty Allowance (on overtime forms)
NDANebraska Dietetic Association
NDANebraska Dressage Association
NDANational Distribution Authority
NDANatural Disaster Assistance
NDANational Dealers Association
NDANormal Daily Activity
NDANational Diploma of Agriculture (UK)
NDANetwork Design Activity
NDANew Dimensional Applications (SAP)
NDANevada Department of Agriculture (est. 1915)
NDANigerian Defence Academy (est. 1964)


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References in periodicals archive?   Acronyms browser?   Full browser?
Coverage includes an introductory overview; individual chapters on the most common types of submissions--FDA meeting requests, orphan drug applications, investigational new drug applications (INDs), new drug applications (NDAs), 505(b)2 NDAs, abbreviated new drug applications (ANDAs), and annual reports; a comparison of the FDA process with those used in Canada, the European Union, Japan, and Australia; and a discussion of the future of drug regulatory submissions.
Adams filed the lawsuit in response to Perrigo's notification that it filed a Paragraph IV Certification in connection with its Abbreviated New Drug Application (ANDA), which seeks FDA approval to engage in the commercial manufacture, use or sale of guaifenesin 600 mg single-ingredient, extended-release tablets (equivalent to Adams' Mucinex SE), prior to the expiration of the '252 patent.
Nabi filed the lawsuit on the basis that Roxane's submission of an Abbreviated New Drug Application (ANDA) with the FDA and its proposed generic product infringe on a patent held by the company that expires in 2021.
 
 
 
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