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Serving hundreds of leading biopharmaceutical companies globally:

Daiichi Sankyo
Dow
US Department of Justice
Merck
McKesson
Chubb
Fuji
Teva
Moodys

Generated: May 28, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 016912

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NDA 016912 describes LARODOPA, which is a drug marketed by Roche and is included in one NDA. Additional details are available on the LARODOPA profile page.

The generic ingredient in LARODOPA is levodopa. There are eighteen drug master file entries for this compound. Additional details are available on the levodopa profile page.
Summary for 016912
Tradename:LARODOPA
Applicant:Roche
Ingredient:levodopa
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 016912

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength250MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength100MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength250MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

UBS
Moodys
Teva
Boehringer Ingelheim
QuintilesIMS
Cerilliant
AstraZeneca
Queensland Health
Accenture

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