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Federal Trade Commission
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Generated: January 16, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070107

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NDA 070107 describes PROPACET 100, which is a drug marketed by Teva and is included in one NDA. Additional details are available on the PROPACET 100 profile page.

The generic ingredient in PROPACET 100 is acetaminophen; propoxyphene napsylate. There are sixty-six drug master file entries for this compound. Additional details are available on the acetaminophen; propoxyphene napsylate profile page.
Summary for 070107
Tradename:PROPACET 100
Applicant:Teva
Ingredient:acetaminophen; propoxyphene napsylate
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength650MG;100MG
Approval Date:Jun 12, 1985TE:RLD:No

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Accenture
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Queensland Health

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verifification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.

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