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Dow
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Generated: April 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 074711

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NDA 074711 describes MEXILETINE HYDROCHLORIDE, which is a drug marketed by Idt Australia Ltd, Teva, and Watson Labs, and is included in four NDAs. It is available from four suppliers. Additional details are available on the MEXILETINE HYDROCHLORIDE profile page.

The generic ingredient in MEXILETINE HYDROCHLORIDE is mexiletine hydrochloride. There are five drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the mexiletine hydrochloride profile page.
Summary for 074711
Tradename:MEXILETINE HYDROCHLORIDE
Applicant:Watson Labs
Ingredient:mexiletine hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 074711

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength150MG
Approval Date:Feb 26, 1997TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength200MG
Approval Date:Feb 26, 1997TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength250MG
Approval Date:Feb 26, 1997TE:RLD:No

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Farmers Insurance
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