Thursday 29 September 2016

Vendrex




Vendrex may be available in the countries listed below.


Ingredient matches for Vendrex



Diclofenac

Diclofenac sodium salt (a derivative of Diclofenac) is reported as an ingredient of Vendrex in the following countries:


  • Brazil

International Drug Name Search

Wednesday 28 September 2016

Cubicin


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


CUBICIN (daptomycin - injectable; iv (infusion))



  • Manufacturer: CUBIST

    Approval date: September 12, 2003

    Strength(s): 500MG/VIAL [RLD]

Has a generic version of Cubicin been approved?


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


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




  • Methods for administration of antibiotics
    Patent 6,468,967
    Issued: October 22, 2002
    Inventor(s): Frederick B.; Oleson, Jr. & Francis P.; Tally
    Assignee(s): Cubist Pharmaceuticals, Incorporated
    The invention provides methods for administering a therapeutically effective amount of daptomycin while minimizing skeletal muscle toxicity. The methods provide daptomycin administration at a dosing interval of 24 hours or greater. This long dosing interval minimizes skeletal muscle toxicity and allows for higher peak concentrations of daptomycin, which is related to daptomycin's efficacy. The invention also provides methods of administering lipopeptide antibiotics other than daptomycin while minimizing skeletal muscle toxicity by administering a therapeutically effective amount of the lipopeptide antibiotic at a dosage interval that does not result in muscle toxicity. The invention also provides methods of administering quinupristin/dalfopristin while minimizing skeletal muscle toxicity by administering a therapeutically effective amount of quinupristin/dalfopristin at a dosage interval that does not result in muscle toxicity.
    Patent expiration dates:

    • September 24, 2019
      ✓ 
      Patent use: METHOD OF TREATING BACTERIAL INFECTIONS




  • Methods for administration of antibiotics
    Patent 6,852,689
    Issued: February 8, 2005
    Inventor(s): Oleson, Jr.; Frederick B. & Tally; Francis P.
    Assignee(s): Cubist Pharmaceuticals, Inc.
    The invention provides methods for administering a therapeutically effective amount of daptomycin while minimizing skeletal muscle toxicity. The methods provide daptomycin administration at a dosing interval of 24 hours or greater. This long dosing interval minimizes skeletal muscle toxicity and allows for higher peak concentrations of daptomycin, which is related to daptomycin's efficacy. The invention also provides methods of administering lipopeptide antibiotics other than daptomycin while minimizing skeletal muscle toxicity by administering a therapeutically effective amount of the lipopeptide antibiotic at a dosage interval that does not result in muscle toxicity. The invention also provides methods of administering quinupristin/dalfopristin while minimizing skeletal muscle toxicity by administering a therapeutically effective amount of quinupristin/dalfopristin at a dosage interval that dos not result in muscle toxicity.
    Patent expiration dates:

    • September 24, 2019
      ✓ 
      Patent use: METHOD OF TREATING BACTERIAL INFECTIONS




  • Daptomycin for the treatment of biofilm and catheter salvage
    Patent 8,003,673
    Issued: August 23, 2011
    Inventor(s): Alder; Jeffrey & Silverman; Jared & Mortin; Lawrence & Van Praagh; Andrew
    Assignee(s): Cubist Pharmaceuticals, Inc.
    Daptomycin can be used for biofilm treatment (particularly central venous catheter salvage for S. epidermidis infected catheters). Catheter salvage with daptomycin shows rapid cidality, activity against stationary phase bacteria, and penetration and activity in biofilms. The present inventions provide formulations, methods, and articles of manufacture useful for biofilm treatment or catheter salvage involving daptomycin. Particular formulations include daptomycin in lactated Ringer's solution having a rapid kill curve against the bacteria of the biofilm.
    Patent expiration dates:

    • September 4, 2028
      ✓ 
      Patent use: TREATMENT OF THE FOLLOWING INFECTIONS: COMPLICATED SKIN AND SKIN STRUCTURE INFECTIONS AND STAPHYLOCOCCUS AUREUS BLOODSTREAM INFECTIONS (BACTEREMIA) INCLUDING THOSE WITH RIGHT-SIDED INFECTIVE ENDOCARDITIS




  • High purity lipopeptides
    Patent 8,058,238
    Issued: November 15, 2011
    Inventor(s): Kelleher; Thomas & Lai; Jan-Ji & DeCourcey; Joseph P. & Lynch; Paul & Zenoni; Maurizio & Tagliani; Auro
    Assignee(s): Cubist Pharmaceuticals, Inc.
    The invention discloses highly purified daptomycin and to pharmaceutical compositions comprising this compound. The invention discloses a method of purifying daptomycin comprising the sequential steps of anion exchange chromatography, hydrophobic interaction chromatography and anion exchange chromatography. The invention also discloses a method of purifying daptomycin by modified buffer enhanced anion exchange chromatography. The invention also discloses an improved method for producing daptomycin by fermentation of Streptomyces roseosporus. The invention also discloses high pressure liquid chromatography methods for analysis of daptomycin purity. The invention also discloses lipopeptide micelles and methods of making the micelles. The invention also discloses methods of using lipopeptide micelles for purifying lipopeptide antibiotics, such as daptomycin. The invention also discloses using lipopeptide micelles therapeutically.
    Patent expiration dates:

    • November 28, 2020
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Anhydro-and isomer-a-21978c cyclic peptides
    Patent RE39071
    Issued: April 18, 2006
    Inventor(s): Baker; Patrick J. & Debono; Manuel & Farid; Khadiga Z. & Molloy; R. Michael
    Assignee(s): Eli Lilly and Company
    Two new groups of A-21978C cyclic peptides, anhydro- and isomer-A21978C peptide derivatives, have antibacterial activity and are useful as intermediates. The two groups are prepared via transpeptidation of the parent cyclic peptides. Pharmaceutical formulations containing the new peptides as active ingredients and methods of treating infections caused by susceptible Gram-positive bacteria with the formulations are also provided. The invention also provides an antibacterial composition containing the new drug substance LY 146032 in substantially pure form.
    Patent expiration dates:

    • June 15, 2016
      ✓ 
      Patent use: METHOD FOR TREATING BACTERIAL INFECTION
      ✓ 
      Drug substance
      ✓ 
      Drug product



See also...

  • Cubicin Consumer Information (Drugs.com)
  • Cubicin Consumer Information (Wolters Kluwer)
  • Cubicin Consumer Information (Cerner Multum)
  • Cubicin Advanced Consumer Information (Micromedex)
  • Cubicin AHFS DI Monographs (ASHP)
  • Daptomycin Consumer Information (Wolters Kluwer)
  • Daptomycin Consumer Information (Cerner Multum)
  • Daptomycin Intravenous Advanced Consumer Information (Micromedex)
  • Daptomycin AHFS DI Monographs (ASHP)

Cordarone


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


CORDARONE (amiodarone hydrochloride - tablet; oral)



  • Manufacturer: WYETH PHARMS INC

    Approval date: December 24, 1985

    Strength(s): 200MG [RLD][AB]

Has a generic version of Cordarone been approved?


Yes. The following products are equivalent to Cordarone:


amiodarone hydrochloride tablet; oral



  • Manufacturer: APOTEX CORP

    Approval date: November 6, 2008

    Strength(s): 200MG [AB]


  • Manufacturer: AUROSAL PHARMS

    Approval date: April 8, 2005

    Strength(s): 200MG [AB]


  • Manufacturer: BARR

    Approval date: January 25, 2001

    Strength(s): 200MG [AB]


  • Manufacturer: MYLAN

    Approval date: February 24, 1999

    Strength(s): 200MG [AB]


  • Manufacturer: SANDOZ

    Approval date: December 23, 1998

    Strength(s): 200MG [AB]


  • Manufacturer: TARO

    Approval date: March 30, 2001

    Strength(s): 200MG [AB]


  • Manufacturer: TEVA PHARMS

    Approval date: November 30, 1998

    Strength(s): 200MG [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: September 16, 2008

    Strength(s): 200MG [AB]

PACERONE (amiodarone hydrochloride tablet; oral)



  • Manufacturer: UPSHER SMITH

    Approval date: April 30, 1998

    Strength(s): 200MG [AB]

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

There are no current U.S. patents associated with Cordarone.

See also...

  • Cordarone Consumer Information (Wolters Kluwer)
  • Cordarone Consumer Information (Cerner Multum)
  • Cordarone Advanced Consumer Information (Micromedex)
  • Amiodarone Consumer Information (Drugs.com)
  • Amiodarone Consumer Information (Wolters Kluwer)
  • Amiodarone Solution Consumer Information (Wolters Kluwer)
  • Amiodarone Consumer Information (Cerner Multum)
  • Amiodarone injection Consumer Information (Cerner Multum)
  • Amiodarone Intravenous Advanced Consumer Information (Micromedex)
  • Amiodarone Intravenous, Oral Advanced Consumer Information (Micromedex)
  • Amiodarone Hydrochloride AHFS DI Monographs (ASHP)

Ran-Lansoprazole




Ran-Lansoprazole may be available in the countries listed below.


Ingredient matches for Ran-Lansoprazole



Lansoprazole

Lansoprazole is reported as an ingredient of Ran-Lansoprazole in the following countries:


  • South Africa

International Drug Name Search

Piperazin




Piperazin may be available in the countries listed below.


Ingredient matches for Piperazin



Piperazine

Piperazine hexahydrate (a derivative of Piperazine) is reported as an ingredient of Piperazin in the following countries:


  • Venezuela

International Drug Name Search

Ramipril / HCT Hexal




Ramipril/HCT Hexal may be available in the countries listed below.


Ingredient matches for Ramipril/HCT Hexal



Hydrochlorothiazide

Hydrochlorothiazide is reported as an ingredient of Ramipril/HCT Hexal in the following countries:


  • Austria

Ramipril

Ramipril is reported as an ingredient of Ramipril/HCT Hexal in the following countries:


  • Austria

International Drug Name Search

Loxiflam




Loxiflam may be available in the countries listed below.


Ingredient matches for Loxiflam



Meloxicam

Meloxicam is reported as an ingredient of Loxiflam in the following countries:


  • South Africa

International Drug Name Search