Thursday, 10 June 2010

Cymbalta


Cymbalta is a brand name of duloxetine, approved by the FDA in the following formulation(s):


CYMBALTA (duloxetine hydrochloride - capsule, delayed rel pellets; oral)



  • Manufacturer: LILLY

    Approval date: August 3, 2004

    Strength(s): EQ 20MG BASE, EQ 30MG BASE, EQ 60MG BASE [RLD]

Has a generic version of Cymbalta been approved?


No. There is currently no therapeutically equivalent version of Cymbalta available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cymbalta. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • 3-aryloxy-3-substituted propanamines
    Patent 5,023,269
    Issued: June 11, 1991
    Inventor(s): Robertson; David W. & Wong; David T. & Krushinski, Jr.; Joseph H.
    Assignee(s): Eli Lilly and Company
    The present invention provides 3-aryloxy-3-substituted propanamines capable of inhibiting the uptake of serotonin and norepinephrine.
    Patent expiration dates:

    • June 11, 2013
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      Patent use: METHOD FOR INHIBITING SEROTONIN UPTAKE
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: MANAGEMENT OF FIBROMYALGIA (FM)
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: TREATMENT OF MAJOR DEPRESSIVE DISORDER (MDD)
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: MANAGEMENT OF CHRONIC MUSCULOSKELETAL PAIN
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      Drug substance
      ✓ 
      Drug product


    • June 11, 2013
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      Patent use: METHOD OF TREATING ANXIETY
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: METHOD OF TREATING DEPRESSION
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: METHOD FOR INHIBITING NOREPINEPHRINE UPTAKE
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: TREATMENT OF GENERALIZED ANXIETY DISORDER
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      Drug substance
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      Drug product


    • June 11, 2013
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      Patent use: TREATMENT OF MAJOR DEPRESSIVE DISORDER(MDD);ALTHOUGH THE MEHCHANISM OF THE ANTIDEPRESSANT ACTION OF DULOXETINE IN HUMANS IS UNKNOWN, IT IS BELIEVED TO BE RELATED TO ITS POTENTIATION OF SERATONERGIC AND NORADRENERGIC ACTIVITY IN THE CNS
      ✓ 
      Drug substance
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      Drug product




  • Duloxetine enteric pellets
    Patent 5,508,276
    Issued: April 16, 1996
    Inventor(s): Anderson; Neil R. & Oren; Peter L. & Ogura; Toshihiro & Fujii; Toshiro
    Assignee(s): Eli Lilly and Company
    Shionogi & Co.
    A superior enteric formulation of the antidepressant drug, duloxetine, is in the form of enteric pellets of which the enteric layer comprises hydroxypropylmethylcellulose acetate succinate.
    Patent expiration dates:

    • July 18, 2014
      ✓ 
      Drug product




  • Treatment of fibromyalgia
    Patent 6,596,756
    Issued: July 22, 2003
    Inventor(s): David Joel; Goldstein & Smriti; Iyengar & Rosa Marie Ademe; Simmons
    Assignee(s): Eli Lilly and Company
    A method of using N-methyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine to treat persistent pain.
    Patent expiration dates:

    • September 10, 2019
      ✓ 
      Patent use: MANAGEMENT OF FIBROMYALGIA (FM)



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • November 28, 2010 - REVISIONS TO PROVIDE FOR RESULTS OF MAINTENANCE DATA IN ADULT PATIENTS WITH MAJOR DEPRESSIVE DISORDER

    • June 13, 2011 - MANAGEMENT OF FIBROMYALGIA

    • November 19, 2012 - MAINTENANCE OF GENERALIZED ANXIETY DISORDER (GAD)

    • November 4, 2013 - MANAGEMENT OF CHRONIC MUSCULOSKELETAL PAIN

See also...

  • Cymbalta Consumer Information (Drugs.com)
  • Cymbalta Delayed-Release Capsules Consumer Information (Wolters Kluwer)
  • Cymbalta Consumer Information (Cerner Multum)
  • Cymbalta Advanced Consumer Information (Micromedex)
  • Cymbalta AHFS DI Monographs (ASHP)
  • Duloxetine Delayed-Release Capsules Consumer Information (Wolters Kluwer)
  • Duloxetine Consumer Information (Cerner Multum)
  • Duloxetine Advanced Consumer Information (Micromedex)
  • Duloxetine AHFS DI Monographs (ASHP)

Tuesday, 8 June 2010

Olyspal




Olyspal may be available in the countries listed below.


Ingredient matches for Olyspal



Budesonide

Budesonide is reported as an ingredient of Olyspal in the following countries:


  • Greece

International Drug Name Search

Miozone




Miozone may be available in the countries listed below.


Ingredient matches for Miozone



Aminophylline

Aminophylline is reported as an ingredient of Miozone in the following countries:


  • Romania

International Drug Name Search

Monday, 7 June 2010

Fentanyl ActavisGroup




Fentanyl ActavisGroup may be available in the countries listed below.


Ingredient matches for Fentanyl ActavisGroup



Fentanyl

Fentanyl is reported as an ingredient of Fentanyl ActavisGroup in the following countries:


  • Netherlands

International Drug Name Search

Dropropizine




Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

R05DB19

CAS registry number (Chemical Abstracts Service)

0017692-31-8

Chemical Formula

C13-H20-N2-O2

Molecular Weight

236

Therapeutic Category

Cough suppressant

Chemical Name

1,2-Propanediol, 3-(4-phenyl-1-piperazinyl)-

Foreign Names

  • Dropropizinum (Latin)
  • Dropropizin (German)
  • Dropropizine (French)
  • Dropropizina (Spanish)

Generic Names

  • Dropropizina (OS: DCIT)
  • Dropropizine (OS: DCF, BAN)
  • Katril (IS)
  • UCB 1967 (IS)

Brand Names

  • Actiribex Tosse
    Johnson & Johnson, Italy


  • Catabex
    UCB, Luxembourg


  • Catabina
    Tecnifar, Portugal


  • Ditustat
    Ivax, Czech Republic; Ivax, Slovakia


  • Domutussina
    Proge, Italy


  • Elisir Terpina (Dropropizine and Terpin hydrate)
    Teofarma, Italy


  • Guaiacalcium Complex (Dropropizine and Sulfogaiacol)
    SIT, Italy


  • Larylin Husten-Stiller
    Cheplapharm, Germany


  • Ribex Tosse
    Pfizer Consumer Health Care, Italy


  • Troferit
    Chinoin, Costa Rica; Chinoin, Dominican Republic; Chinoin, Guatemala; Chinoin, Mexico; Chinoin, Nicaragua; Chinoin, Panama; Chinoin, El Salvador


  • Tussiflex
    Abbott, Brazil


  • Vibral
    Solvay, Brazil

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
DCITDenominazione Comune Italiana
ISInofficial Synonym
OSOfficial Synonym
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Pantorc




Pantorc may be available in the countries listed below.


Ingredient matches for Pantorc



Pantoprazole

Pantoprazole sodium (a derivative of Pantoprazole) is reported as an ingredient of Pantorc in the following countries:


  • Italy

International Drug Name Search

Saturday, 5 June 2010

Tevcocin




In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Tevcocin



Chloramphenicol

Chloramphenicol is reported as an ingredient of Tevcocin in the following countries:


  • United States

International Drug Name Search