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Generated: July 28, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070401

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NDA 070401 describes MECLOFENAMATE SODIUM, which is a drug marketed by Watson Labs, Usl Pharma, Barr, Vitarine, Am Therap, Sandoz, Watson Labs Teva, Par Pharm, and Mylan, and is included in nineteen NDAs. It is available from one supplier. Additional details are available on the MECLOFENAMATE SODIUM profile page.

The generic ingredient in MECLOFENAMATE SODIUM is meclofenamate sodium. There are eight drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the meclofenamate sodium profile page.

Summary for NDA: 070401

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Analgesics
Anti-inflammatory Agents
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 100MG BASE
Approval Date:Nov 25, 1986TE:RLD:No


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Serving 500+ biopharmaceutical companies globally:

Fish and Richardson
Harvard Business School
Farmers Insurance
Colorcon
US Army
AstraZeneca
Medtronic
Moodys
Boehringer Ingelheim
McKinsey

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