Wednesday 25 March 2009

Parodongyl




Parodongyl may be available in the countries listed below.


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

Ingredient matches for Parodongyl



Chlorhexidine

Chlorhexidine digluconate (a derivative of Chlorhexidine) is reported as an ingredient of Parodongyl in the following countries:


  • Germany

International Drug Name Search

Sunday 22 March 2009

Salbutamol Genfar




Salbutamol Genfar may be available in the countries listed below.


Ingredient matches for Salbutamol Genfar



Salbutamol

Salbutamol is reported as an ingredient of Salbutamol Genfar in the following countries:


  • Colombia

  • Ecuador

Salbutamol sulfate (a derivative of Salbutamol) is reported as an ingredient of Salbutamol Genfar in the following countries:


  • Peru

International Drug Name Search

Monday 16 March 2009

Intelence


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


INTELENCE (etravirine - tablet; oral)



  • Manufacturer: TIBOTEC

    Approval date: January 18, 2008

    Strength(s): 100MG


  • Manufacturer: TIBOTEC

    Approval date: December 22, 2010

    Strength(s): 200MG [RLD]

Has a generic version of Intelence been approved?


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


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Intelence. 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.




  • HIV replication inhibiting pyrimidines
    Patent 6,878,717
    Issued: April 12, 2005
    Inventor(s): De Corte; Bart & De Jonge; Marc Rene & Heeres; Jan & Ho; Chih Yung & Janssen; Paul Adriaan Jan & Kavash; Robert W. & Koymans; Lucien Maria Henricus & Kukla; Michael Joseph & Ludovici; Donald William & Van Aken; Koen Jeanne Alfons
    This invention concerns the use of compounds of formula: the N-oxides, the pharmaceutically acceptable addition salts, quaternary amines and the stereochemically isomeric forms thereof, wherein -a1=-a2-a3=a4- forms a phenyl, pyridinyl, pyrimidinyl, pyridazinyl or pyrazinyl with the attached vinyl group; n is 0 to 4; and where possible 5; R1 is hydrogen, aryl, formyl, C1-6alkylcarbonyl, C1-6alkyl, C1-6alkyloxy-carbonyl, substituted C1-6alkyl, or substituted C1-6alkyloxyC1-6alkylcarbonyl; each R2 independently is hydroxy, halo, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C3-7cycloalkyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalo-methylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, —NHC(═O)R6, —C(═NH)R6 or a 5-membered heterocyclic ring; p is 1 or 2; L is optionally substituted C1-10alkyl, C2-10alkenyl, C2-10alkynyl or C3-7cycloalkyl; or L is —X—R3 wherein R3 is optionally substituted phenyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl; X is —NR1—, —NH—NH—, —N═N—, —O—, —C(═O)—, —CHOH—, —S—, —S(═O)— or —S(═O)2—; Q is hydrogen, C1-6alkyl, halo, polyhalo-C1-6alkyl or an optionally substituted amino group; Y represents hydroxy, halo, C3-7cycloalkyl, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, —NHC(═O)R6, —C(═NH)R6 or aryl; aryl is optionally substituted phenyl; Het is an optionally substituted heterocyclic radical; for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection.
    Patent expiration dates:

    • November 5, 2019
      ✓ 
      Patent use: TREATMENT OF HIV INFECTION IN COMBINATION WITH ONE OR MORE ADDITIONAL HIV ANTIVIRAL AGENTS


    • November 5, 2019
      ✓ 
      Patent use: IN COMBINATION WITH OTHER ANTIRETROVIRAL AGENTS FOR THE TREATMENT OF HIV-1 INFECTION IN TREATMENT-EXPERIENCED ADULT PATIENTS, WHO HAVE EVIDENCE OF VIRAL REPLICATION AND HIV-1 STRAINS RESISTANT TO AN NNRTI AND OTHER ANTIRETROVIRAL AGENTS




  • HIV replication inhibiting pyrimidines
    Patent 7,037,917
    Issued: May 2, 2006
    Inventor(s): De Corte; Bart & De Jonge; Marc Rene & Heeres; Jan & Ho; Chih Yung & Janssen; Paul Adriaan Jan & Kavash; Robert W. & Koymans; Lucien Maria Henricus & Kukla; Michael Joseph & Ludovici; Donald William & Van Aken; Koen Jeanne Alfons
    Assignee(s): Janssen Pharmaceutica, N.V.
    This invention concerns the use of compounds of formula the N-oxides, the pharmaceutically acceptable addition salts, quaternary amines and the stereochemically isomeric forms thereof, wherein -a1=a2-a3=a4- forms a phenyl, pyridinyl, pyrimidinyl, pyridazinyl or pyrazinyl with the attached vinyl group; n is 0 to 4; and where possible 5; R1 is hydrogen, aryl, formyl, C1-6alkylcarbonyl, C1-6alkyl, C1-6alkyloxycarbonyl, substituted C1-6alkyl, or substituted C1-6alkyloxyC1-6alkylcarbonyl; each R2 independently is hydroxy, halo, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C3-7cycloalkyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, —NHC(═O)R6, —C(═NH)R6 or a 5-membered heterocyclic ring; p is 1 or 2; L is optionally substituted C1-10alkyl, C2-10alkenyl, C2-10alkynyl or C3-7cycloalkyl; or L is —X—R3 wherein R3 is optionally substituted phenyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl; X is —NR1—, —NH—NH—, —N═N—, —O—, —C(═O)—, —CHOH—, —S—, —S(═O)— or —S(═O)2—; Q is hydrogen, C1-6alkyl, halo, polyhalo-C1-6alkyl or an optionally substituted amino group; Y represents hydroxy, halo, C3-7cycloalkyl, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, —NHC(═O)R6, —C(═NH)R6 or aryl; aryl is optionally substituted phenyl; Het is an optionally substituted heterocyclic radical; for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection.
    Patent expiration dates:

    • December 13, 2020
      ✓ 
      Patent use: IN COMBINATION WITH OTHER ANTIRETROVIRAL AGENTS FOR THE TREATMENT OF HIV-1 INFECTION IN TREATMENT-EXPERIENCED ADULT PATIENTS, WHO HAVE EVIDENCE OF VIRAL REPLICATION AND HIV-1 STRAINS RESISTANT TO AN NNRTI AND OTHER ANTIRETROVIRAL AGENTS
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • December 13, 2020
      ✓ 
      Patent use: TREATMENT OF HIV INFECTION IN COMBINATION WITH ONE OR MORE ADDITIONAL HIV ANTIVIRAL AGENTS
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Antiviral compositions
    Patent 7,887,845
    Issued: February 15, 2011
    Inventor(s): Verreck; Geert & Baert; Lieven
    Assignee(s): Janssen Pharmaceutica NV
    The present invention is concerned with pharmaceutical compositions of antiviral compounds which can be administered to a mammal, in particular a human, suffering from a viral infection. These compositions comprise particles obtainable by melt-extruding a mixture comprising one or more antiviral compounds and one or more appropriate water-soluble polymers and subsequently milling said melt-extruded mixture.
    Patent expiration dates:

    • March 25, 2019
      ✓ 
      Drug product




  • HIV replication inhibiting pyrimidines
    Patent 8,003,789
    Issued: August 23, 2011
    Inventor(s): De Corte; Bart & de Jonge; Marc René & Heeres; Jan & Ho; Chih Yung & Janssen; Paul Adriaan Jan & Kavash; Robert W. & Koymans; Lucien Maria Henricus & Kukla; Michael Joseph & Ludovici; Donald William & Van Aken; Koen Jeanne Alfons & Marcel Andries; Koenraad Jozef Lodewi
    Assignee(s): Janssen Pharmaceutica, N.V.
    This invention concerns the use of compounds of formula the N-oxides, pharmaceutically acceptable addition salts, quaternary amines, stereochemically isomeric forms thereof, wherein -a1=a2-a3=a4- forms phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl with the attached vinyl group; n is 0 to 5; R1 is hydrogen, aryl, formyl, C1-6alkylcarbonyl, C1-6alkyl, C1-6alkyloxycarbonyl, substituted C1-6alkyl, substituted C1-6alkyloxyC1-6alkylcarbonyl; R2 is hydroxy, halo, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C3-7cycloalkyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, —NHC(═O)R6, —C(═NH)R6, 5-membered heterocyclic ring; L is optionally substituted C1-10alkyl, C2-10alkenyl, C2-10alkynyl or C3-7cycloalkyl; or —X—R3; Q is hydrogen, C1-6alkyl, halo, polyhalo-C1-6alkyl, optionally substituted amino group; Y represents hydroxy, halo, C3-7cycloalkyl, optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono-or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)pR6, —NH—S(═O)pR6, —C(═O)R6, —NHC(═O)H, —C(═O)NHNH2, 13 NHC(═O)R6,—C(═NH)R6, aryl; for the treatment of subjects suffering from HIV infection.
    Patent expiration dates:

    • November 1, 2019



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:
    • January 18, 2013 - NEW CHEMICAL ENTITY

See also...

  • Intelence Consumer Information (Drugs.com)
  • Intelence Consumer Information (Wolters Kluwer)
  • Intelence Consumer Information (Cerner Multum)
  • Intelence Advanced Consumer Information (Micromedex)
  • Intelence AHFS DI Monographs (ASHP)
  • Etravirine Consumer Information (Wolters Kluwer)
  • Etravirine Consumer Information (Cerner Multum)
  • Etravirine Advanced Consumer Information (Micromedex)
  • Etravirine AHFS DI Monographs (ASHP)

Sunday 15 March 2009

Noben




Noben may be available in the countries listed below.


Ingredient matches for Noben



Idebenone

Idebenone is reported as an ingredient of Noben in the following countries:


  • Russian Federation

International Drug Name Search

Saturday 14 March 2009

Premature Ventricular Depolarizations Medications


Drugs associated with Premature Ventricular Depolarizations

The following drugs and medications are in some way related to, or used in the treatment of Premature Ventricular Depolarizations. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.





Drug List:

Friday 13 March 2009

Antistrumin




Antistrumin may be available in the countries listed below.


Ingredient matches for Antistrumin



Potassium Iodide

Potassium Iodide is reported as an ingredient of Antistrumin in the following countries:


  • Bulgaria

International Drug Name Search

Sunday 8 March 2009

A-Vite




A-Vite may be available in the countries listed below.


Ingredient matches for A-Vite



Retinol

Retinol is reported as an ingredient of A-Vite in the following countries:


  • Portugal

International Drug Name Search

Friday 6 March 2009

Pyme M-Predni




Pyme M-Predni may be available in the countries listed below.


Ingredient matches for Pyme M-Predni



Methylprednisolone

Methylprednisolone is reported as an ingredient of Pyme M-Predni in the following countries:


  • Vietnam

International Drug Name Search