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Serving hundreds of leading biopharmaceutical companies globally:

Dow
Fuji
Healthtrust
Harvard Business School
Colorcon
QuintilesIMS
Federal Trade Commission
Boehringer Ingelheim
Chubb

Generated: April 23, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076184

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NDA 076184 describes ALENDRONATE SODIUM, which is a drug marketed by West-ward Pharms Int, Apotex, Aurobindo Pharma, Cipla Ltd, Dr Reddys Labs Ltd, Hangzhou Binjiang, Impax Labs Inc, Jubilant Cadista, Mylan, Sun Pharma Global, Teva Pharms, Upsher-smith Labs, and Watson Labs, and is included in fourteen NDAs. It is available from twenty-three suppliers. Additional details are available on the ALENDRONATE SODIUM profile page.

The generic ingredient in ALENDRONATE SODIUM is alendronate sodium. There are twenty-five drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the alendronate sodium profile page.
Summary for 076184
Tradename:ALENDRONATE SODIUM
Applicant:Teva Pharms
Ingredient:alendronate sodium
Patents:0
Therapeutic Class:Metabolic Bone Disease Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 076184

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 70MG BASE
Approval Date:Feb 6, 2008TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 35MG BASE
Approval Date:Aug 4, 2008TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Mallinckrodt
Chinese Patent Office
UBS
Fuji
US Department of Justice
US Army
Cipla
Fish and Richardson
McKinsey

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