Tuesday, September 27, 2016

Ditropan


See also: Generic Ditropan XL


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


DITROPAN (oxybutynin chloride - tablet; oral)



  • Manufacturer: JANSSEN PHARMS

    Approved Prior to Jan 1, 1982

    Strength(s): 5MG [RLD][AB]

Has a generic version of Ditropan been approved?


Yes. The following products are equivalent to Ditropan:


oxybutynin chloride tablet; oral



  • Manufacturer: PLIVA

    Approval date: November 14, 1988

    Strength(s): 5MG [AB]


  • Manufacturer: USL PHARMA

    Approval date: July 31, 1996

    Strength(s): 5MG [AB]


  • Manufacturer: VINTAGE PHARMS

    Approval date: October 31, 1997

    Strength(s): 5MG [AB]

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

See also...

  • Ditropan Consumer Information (Drugs.com)
  • Ditropan Consumer Information (Wolters Kluwer)
  • Ditropan Syrup Consumer Information (Wolters Kluwer)
  • Ditropan Consumer Information (Cerner Multum)
  • Ditropan Advanced Consumer Information (Micromedex)
  • Oxybutynin Consumer Information (Drugs.com)
  • Oxybutynin Consumer Information (Wolters Kluwer)
  • Oxybutynin Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Oxybutynin Gel Consumer Information (Wolters Kluwer)
  • Oxybutynin Syrup Consumer Information (Wolters Kluwer)
  • Oxybutynin System Consumer Information (Wolters Kluwer)
  • Oxybutynin Consumer Information (Cerner Multum)
  • Oxybutynin topical Consumer Information (Cerner Multum)
  • Oxybutynin transdermal Consumer Information (Cerner Multum)
  • Oxybutynin Advanced Consumer Information (Micromedex)
  • Oxybutynin Transdermal Advanced Consumer Information (Micromedex)
  • Oxybutynin Chloride AHFS DI Monographs (ASHP)

Invega Sustenna


See also: Generic Invega


Invega Sustenna is a brand name of paliperidone, approved by the FDA in the following formulation(s):


INVEGA SUSTENNA (paliperidone palmitate - suspension, extended release; intramuscular)



  • Manufacturer: JANSSEN PHARMS

    Approval date: July 31, 2009

    Strength(s): 117MG/0.75ML (117MG/0.75ML) [RLD], 156MG/ML (156MG/ML), 234MG/1.5ML (156MG/ML), 39MG/0.25ML (39MG/0.25ML), 78MG/0.5ML (78MG/0.5ML)

Has a generic version of Invega Sustenna been approved?


No. There is currently no therapeutically equivalent version of Invega Sustenna available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Invega Sustenna. 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-piperidinyl-1,2-benzisoxazoles
    Patent 5,254,556
    Issued: October 19, 1993
    Inventor(s): Janssen; Cornelus G. M. & Knaeps; Alfonsus G. & Kennis; Ludo E. J. & Vandenberk; Jan
    Assignee(s): Janssen Pharmaceutica N.V.
    The invention relates to C.sub.2-20 alkanoic acid esters of 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6, 7,8,9-tetrahydro-9-hydroxy-2 -methyl-4H-pyrido[1,2-a]pyrimidin-4-one, pharmaceutically acceptable acid addition salts thereof, and enantiomeric forms thereof, which are useful in the treatment of warm-blooded animals suffering from psychotic diseases.
    Patent expiration dates:

    • October 27, 2012
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • April 27, 2013
      ✓ 
      Pediatric exclusivity




  • Use of purified surface modifiers to prevent particle aggregation during sterilization
    Patent 5,352,459
    Issued: October 4, 1994
    Inventor(s): Hollister; Kenneth R. & Ladd; David & McIntire; Gregory L. & Na; George C. & Rajagopalan; Natarajan & Yuan; Barbara O.
    Assignee(s): Sterling Winthrop Inc.
    This invention discloses a composition comprised of nanoparticles having a purified polymeric surfactant as a surface modifier adsorbed on the surface thereof and a cloud point modifier associated therewith, which cloud point modifier is present in an amount sufficient to increase the cloud point of the surface modifier. Preferred purified polymeric surfactants are purified polyalkyleneoxide substituted ethylenediamine surfactants. A preferred cloud point modifier is polyethylene glycol. This invention further discloses a method of making nanoparticles having a purified polymeric surfactant as a surface modifier adsorbed on the surface and a cloud point modifier associated therewith, comprised of contacting said nanoparticles with the cloud point modifier for a time and under conditions sufficient to increase the cloud point of the surface modifier.
    Patent expiration dates:

    • December 16, 2012
      ✓ 
      Drug product


    • June 16, 2013
      ✓ 
      Pediatric exclusivity




  • Aqueous suspensions of 9-hydroxyrisperidone fatty acid esters
    Patent 6,077,843
    Issued: June 20, 2000
    Inventor(s): Fran.cedilla.ois; Marc Karel Jozef & Embrechts; Roger Carolus Augusta & Borghijs; Herman Karel & Monbaliu; Johan
    Assignee(s): Janssen Pharmaceutica, N.V.
    The present invention is concerned with a pharmaceutical composition suitable as a depot formulation for administration via intramuscular or subcutaneous injection, comprising: (1) as an active ingredient a therapeutically effective amount of a 9-hydroxyrisperidone fatty acid ester or a salt, or a stereoisomer or a stereoisomeric mixture thereof and (2) a pharmaceutically acceptable carrier; wherein the pharmaceutically acceptable carrier is water and the active ingredient is suspended therein; and with a process of preparing such a composition. The invention further concerns such a pharmaceutical composition for use as a medicament in the treatment of schizophrenia, non-schizophrenic psychoses, behavioural disturbances associated with neurodegenerative disorders, e.g. in dementia, behavioural disturbances in mental retardation and autism, bipolar mania, depression, anxiety.
    Patent expiration dates:

    • May 12, 2017
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA
      ✓ 
      Drug product


    • November 12, 2017
      ✓ 
      Pediatric exclusivity




  • Aqueous suspensions of submicron 9-hydroxyrisperidone fatty acid esters
    Patent 6,555,544
    Issued: April 29, 2003
    Inventor(s): Marc Karel Jozef; François & Willy Maria Albert Carlo; Dries & Esther Dina Guido; Basstanie
    Assignee(s): Janssen Pharmaceutica, N.V.
    The present invention is concerned with a pharmaceutical composition suitable as a depot formulation for administration via intramuscular or subcutaneous injection, comprising: (1) as an active ingredient a therapeutically effective amount of a 9-hydroxy-risperidone fatty acid ester or a salt, or a stereoisomer or a stereoisomeric mixture thereof in submicron form and (2) a pharmaceutically acceptable carrier; wherein the pharmaceutically acceptable carrier is water and the active ingredient is suspended therein: and with a process of preparing such a composition. The invention further concerns such a pharmaceutical composition for use as a medicament in the treatment of psychosis, schizophrenia, schizoaffective disorders, non-schizophrenic psychoses, behavioural disturbances associated with neurodegenerative disorders, e.g. in dementia, behavioural disturbances in mental retardation and autism, Tourette's syndrome, bipolar mania, depression, anxiety.
    Patent expiration dates:

    • November 10, 2018
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA
      ✓ 
      Drug product


    • May 10, 2019
      ✓ 
      Pediatric exclusivity



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:
    • December 19, 2011 - NEW CHEMICAL ENTITY

    • June 19, 2012 - PEDIATRIC EXCLUSIVITY

    • July 31, 2012 - NEW DOSAGE FORM

    • January 31, 2013 - PEDIATRIC EXCLUSIVITY

See also...

  • Invega Sustenna Consumer Information (Wolters Kluwer)
  • Invega Sustenna Advanced Consumer Information (Micromedex)
  • Paliperidone Consumer Information (Wolters Kluwer)
  • Paliperidone Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Paliperidone Consumer Information (Cerner Multum)
  • Paliperidone Advanced Consumer Information (Micromedex)
  • Paliperidone Intramuscular Advanced Consumer Information (Micromedex)
  • Paliperidone AHFS DI Monographs (ASHP)

Daraprim


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


DARAPRIM (pyrimethamine - tablet; oral)



  • Manufacturer: COREPHARMA

    Approved Prior to Jan 1, 1982

    Strength(s): 25MG [RLD]

Has a generic version of Daraprim been approved?


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


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

See also...

  • Daraprim Consumer Information (Wolters Kluwer)
  • Daraprim Consumer Information (Cerner Multum)
  • Daraprim Advanced Consumer Information (Micromedex)
  • Pyrimethamine Consumer Information (Wolters Kluwer)
  • Pyrimethamine Consumer Information (Cerner Multum)
  • Pyrimethamine Advanced Consumer Information (Micromedex)

Depen


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


DEPEN (penicillamine - tablet; oral)



  • Manufacturer: MEDA PHARMS

    Approved Prior to Jan 1, 1982

    Strength(s): 250MG [RLD]

Has a generic version of Depen been approved?


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


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

See also...

  • Depen Consumer Information (Wolters Kluwer)
  • Depen Consumer Information (Cerner Multum)
  • Depen Advanced Consumer Information (Micromedex)
  • Penicillamine Consumer Information (Wolters Kluwer)
  • Penicillamine Consumer Information (Cerner Multum)
  • Penicillamine Advanced Consumer Information (Micromedex)
  • Penicillamine AHFS DI Monographs (ASHP)

Benzamycin Pak


See also: Generic Benzamycin


Benzamycin Pak is a brand name of benzoyl peroxide/erythromycin topical, approved by the FDA in the following formulation(s):


BENZAMYCIN PAK (benzoyl peroxide; erythromycin - gel; topical)



  • Manufacturer: SANOFI AVENTIS US

    Approval date: November 27, 2000

    Strength(s): 5%;3% [RLD]

Has a generic version of Benzamycin Pak been approved?


No. There is currently no therapeutically equivalent version of Benzamycin Pak available.


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

See also...

  • Benzamycin Pak Gel Consumer Information (Wolters Kluwer)
  • Benzamycin Pak Topical Advanced Consumer Information (Micromedex)
  • Benzoyl Peroxide/Erythromycin Gel Consumer Information (Wolters Kluwer)
  • Benzoyl peroxide and erythromycin topical Consumer Information (Cerner Multum)
  • Erythromycin and benzoyl peroxide Topical Advanced Consumer Information (Micromedex)

Desferal


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


DESFERAL (deferoxamine mesylate - injectable; injection)



  • Manufacturer: NOVARTIS

    Approved Prior to Jan 1, 1982

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


  • Manufacturer: NOVARTIS

    Approval date: May 25, 2000

    Strength(s): 2GM/VIAL [RLD][AP]

Has a generic version of Desferal been approved?


Yes. The following products are equivalent to Desferal:


deferoxamine mesylate injectable; injection



  • Manufacturer: APP PHARMS

    Approval date: September 15, 2009

    Strength(s): 2GM/VIAL [AP], 500MG/VIAL [AP]


  • Manufacturer: BEDFORD

    Approval date: May 30, 2007

    Strength(s): 2GM/VIAL [AP], 500MG/VIAL [AP]


  • Manufacturer: HOSPIRA

    Approval date: March 17, 2004

    Strength(s): 2GM/VIAL [AP], 500MG/VIAL [AP]


  • Manufacturer: WATSON LABS

    Approval date: March 31, 2006

    Strength(s): 2GM/VIAL [AP], 500MG/VIAL [AP]

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

See also...

  • Desferal Consumer Information (Wolters Kluwer)
  • Desferal Consumer Information (Cerner Multum)
  • Desferal Advanced Consumer Information (Micromedex)
  • Desferal AHFS DI Monographs (ASHP)
  • Deferoxamine Consumer Information (Wolters Kluwer)
  • Deferoxamine Consumer Information (Cerner Multum)
  • Deferoxamine Injection Advanced Consumer Information (Micromedex)
  • Deferoxamine Mesylate AHFS DI Monographs (ASHP)

Denavir


Denavir is a brand name of penciclovir topical, approved by the FDA in the following formulation(s):


DENAVIR (penciclovir sodium - cream; topical)



  • Manufacturer: DENCO ASSET

    Approval date: September 24, 1996

    Strength(s): 1% [RLD]

Has a generic version of Denavir been approved?


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


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




  • Treatment of a latent infection of herpes viruses
    Patent 5,840,763
    Issued: November 24, 1998
    Inventor(s): Field; Hugh John & Thackray; Alana Maureen & Bacon; Teresa Helen & Sutton; David & Vere Hodge; Richard Anthony
    Assignee(s): SmithKline Beecham plc
    A method for the treatment of latent infection of herpesviruses in mammals, including humans, which method comprises administering to the mammal in need of such treatment, an effective amount of a compound of formula (A): ##STR1## or a bioprecursor, or a pharmaceutically acceptable salt, phosphate ester and/or acyl derivative of either of the foregoing.
    Patent expiration dates:

    • September 1, 2015
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS




  • Penciclovir for the treatment of post therapeutic neuralgia
    Patent 5,866,581
    Issued: February 2, 1999
    Inventor(s): Boon; Ronald James & Griffin; David Ronald John
    Assignee(s): SmithKline Beecham p.l.c.
    A method for the treatment of PHN in mammals, including humans, which method comprises administering an effective amount of a compound of formula (A), or a pharmaceutically acceptable salt thereof. ##STR1##
    Patent expiration dates:

    • October 4, 2014
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS




  • Treatment of a latent infection of herpes virus
    Patent 5,916,893
    Issued: June 29, 1999
    Inventor(s): Field; Hugh John & Thackray; Alana Maureen & Bacon; Teresa Helen & Sutton; David & Vere Hodge; Richard Anthony
    Assignee(s): SmithKline Beecham p.l.c.
    A method for the treatment of latent infection of herpesviruses in mammals, including humans, which method comprises administering to the mammal in need of such treatment, an effective amount of a compound of formula (A): ##STR1## or a bioprecursor, or a pharmaceutically acceptable salt, phosphate ester and/or acyl derivative of either of the foregoing.
    Patent expiration dates:

    • September 1, 2015
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS




  • Penciclovir for the treatment of zoster associated pain
    Patent 6,124,304
    Issued: September 26, 2000
    Inventor(s): Boon; Ronald James & Griffin; David Ronald John
    Assignee(s): SmithKline Beecham PLC
    A method for the treatment of ZAP, in particular PHN, in mammals, including humans, which method comprises administering to the mammal in need of such treatment, an effective amount of penciclovir or famciclovir, or a pharmaceutically acceptable salt thereof.
    Patent expiration dates:

    • October 4, 2014
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS




  • Pharmaceutical formulation
    Patent 6,469,015
    Issued: October 22, 2002
    Inventor(s): Hazel-Ann; Griffiths & Alan John; Goodall & Joshua; Oduro-Yeboah
    Assignee(s): Novartis International Pharmaceutical Ltd
    An oil-in-water topical pharmaceutical formulation or an aqueous formulation for the treatment of virus infections of the skin or mucosa, comprising at least 30% of propylene glycol and solubilized penciclovir.
    Patent expiration dates:

    • October 22, 2019
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS




  • Antiviral guanine derivatives
    Patent 6,579,981
    Issued: June 17, 2003
    Inventor(s): Richard Lewis; Jarvest & Michael Raymond; Harnden
    Assignee(s): Novartis International Pharmaceutical Ltd.
    A compound of formula (I) or a salt or acyl derivative thereof, in which X represents chlorine, C1-6 alkoxy, phenoxy, phenyl C1-6 alkoxy, NH2, —OH or —SH, is useful in treating viral infections.
    Patent expiration dates:

    • June 17, 2020
      ✓ 
      Patent use: TREATMENT OF RECURRENT HERPES LABIALIS (COLD SORES) IN ADULTS



See also...

  • Denavir Consumer Information (Drugs.com)
  • Denavir Consumer Information (Wolters Kluwer)
  • Denavir Consumer Information (Cerner Multum)
  • Denavir Topical Advanced Consumer Information (Micromedex)
  • Denavir AHFS DI Monographs (ASHP)
  • Penciclovir Consumer Information (Wolters Kluwer)
  • Penciclovir topical Consumer Information (Cerner Multum)
  • Penciclovir Topical Advanced Consumer Information (Micromedex)
  • Penciclovir AHFS DI Monographs (ASHP)