Wednesday, September 28, 2016

Viagra


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


VIAGRA (sildenafil citrate - tablet; oral)



  • Manufacturer: PFIZER IRELAND

    Approval date: March 27, 1998

    Strength(s): EQ 100MG BASE [RLD], EQ 25MG BASE, EQ 50MG BASE

Has a generic version of Viagra been approved?


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


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




  • Pyrazolopyrimidinone antianginal agents
    Patent 5,250,534
    Issued: October 5, 1993
    Inventor(s): Bell; Andrew S. & Brown; David & Terrett; Nicholas K.
    Assignee(s): Pfizer Inc.
    Compounds of the formula: ##STR1## wherein R.sup.1 is H, C.sub.1 -C.sub.3 alkyl, C.sub.3 -C.sub.5 cycloalkyl or C.sub.1 -C.sub.3 perfluoroalkyl; R.sup.2 is H, C.sub.1 -C.sub.6 alkyl optionally substituted by OH, C.sub.1 -C.sub.3 alkoxy or C.sub.3 -C.sub.6 cycloalkyl, or C.sub.1 -C.sub.3 perfluoroalkyl; R.sup.3 is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 alkenyl, C.sub.3 -C.sub.6 alkynyl, C.sub.3 -C.sub.7 cycloalkyl, C.sub.1 -C.sub.6 perfluoroalkyl or (C.sub.3 -C.sub.6 cycloalkyl)C.sub.1 -C.sub.6 alkyl; R.sup.4 taken together with the nitrogen atom to which it is attached completes a pyrrolidinyl, piperidino, morpholino, or 4-N-(R.sup.6)-piperazinyl group; R.sup.5 is H, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.3 alkoxy, NR.sup.7 R.sup.8, or CONR.sup.7 R.sup.8 ; R.sup.6 is H, C.sub.1 -C.sub.6 alkyl, (C.sub.1 -C.sub.3 alkoxy) C.sub.2 - C.sub.6 alkyl, hydroxy C.sub.2 -C.sub.6 alkyl, (R.sup.7 R.sup.8 N)C.sub.2 -C.sub.6 alkyl, (R.sup.7 R.sup.8 NCO)C.sub.1 -C.sub.6 alkyl, CONR.sup.7 R.sup.8, CSNR.sup.7 R.sup.8 or C(NH)NR.sup.7 R.sup.8 ; R.sup.7 and R.sup.8 are each independently H, C.sub.1 -C.sub.4 alkyl, (C.sub.1 -C.sub.3 alkoxy)C.sub.2 -C.sub.4 alkyl or hydroxy C.sub.2 -C.sub.4 alkyl; and pharmaceutically acceptable salts thereof, are selective cGMP PDE inhibitors useful in the treatment of cardiovascular disorders such as angina, hypertension, heart failure and atherosclerosis.
    Patent expiration dates:

    • March 27, 2012


    • September 27, 2012
      ✓ 
      Pediatric exclusivity




  • Pyrazolopyrimidinones for the treatment of impotence
    Patent 6,469,012
    Issued: October 22, 2002
    Inventor(s): Peter; Ellis & Nicholas Kenneth; Terrett
    Assignee(s): Pfizer Inc
    The use of a compound of formula (I) wherein R1 is H; C1-C3 alkyl; C1-C3 perfluoroalkyl; or C3-C5 cycloalkyl; R2 is H; optionally substituted C1-C6 alkyl; C1-C3 perfluoroalkyl; or C3-C6 cycloalkyl; R3 is optionally substituted C1-C6 alkyl; C1-C6 perfluoroalkyl; C3-C5 cycloalkyl; C3-C6 alkenyl; or C3-C6 alkynyl; R4 is optionally substituted C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkanoyl, (hydroxy)C2-C4 alkyl or (C2-C3 alkoxy)C1-C2 alkyl; CONR5R6; CO2R7; halo; NR5R6; NHSO2NR5R6; NHSO2R8; SO2NR9R10; or phenyl, pyridyl, pyrimidinyl, imidazolyl, oxazolyl, thiazolyl, thienyl or triazolyl any of which is optionally substituted with methyl; R5 and R6 are each independently H or C1-C4 alkyl, or together with the nitrogen atom to which they are attached form an optionally substituted pyrrolidinyl, piperidino, morpholino, 4-N(R11)-piperazinyl or imidazolyl group; R7 is H or C1-C4 alkyl; R8 is optionally substituted C1-C3 alkyl; R9 and R10 together with the nitrogen atom to which they are attached form an optionally substituted pyrrolidinyl, piperidino, morpholino or 4-N(R12)-piperazinyl group; R11 is H; optionally substituted C1-C3 alkyl; (hydroxy)C2-C3 alkyl; or C1-C4 alkanoyl; R12 is H; optionally substituted C1-C6 alkyl; CONR13R14; CSNR13R14; or C(NH)NR13R14; and R?13? and R14 are each independently H; C1-C4 alkyl; or substituted C2-C4 alkyl; or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition containing either entity, for the manufacture of a medicament for the curative or prophylactic treatment of erectile dysfunction in a male animal, including man; a pharmaceutical composition for said treatment; and a method of said treatment of said male animal with said pharmaceutical composition or with said either entity.
    Patent expiration dates:

    • October 22, 2019
      ✓ 
      Patent use: TREATMENT OF ERECTILE DYSFUNCTION


    • April 22, 2020
      ✓ 
      Pediatric exclusivity



See also...

  • Viagra Consumer Information (Drugs.com)
  • Viagra Consumer Information (Wolters Kluwer)
  • Viagra Consumer Information (Cerner Multum)
  • Viagra Advanced Consumer Information (Micromedex)
  • Sildenafil Consumer Information (Wolters Kluwer)
  • Sildenafil Injection Consumer Information (Wolters Kluwer)
  • Sildenafil Consumer Information (Cerner Multum)
  • Sildenafil Advanced Consumer Information (Micromedex)
  • Sildenafil Intravenous Advanced Consumer Information (Micromedex)
  • Sildenafil Citrate AHFS DI Monographs (ASHP)

Bupivacaine Hydrochloride Baxter




Bupivacaine Hydrochloride Baxter may be available in the countries listed below.


Ingredient matches for Bupivacaine Hydrochloride Baxter



Bupivacaine

Bupivacaine hydrochloride (a derivative of Bupivacaine) is reported as an ingredient of Bupivacaine Hydrochloride Baxter in the following countries:


  • Greece

International Drug Name Search

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)

Dilacor XR


Dilacor XR is a brand name of diltiazem, approved by the FDA in the following formulation(s):


DILACOR XR (diltiazem hydrochloride - capsule, extended release; oral)



  • Manufacturer: WATSON LABS

    Approval date: May 29, 1992

    Strength(s): 120MG [AB2], 180MG [AB2], 240MG [RLD][AB2]

Has a generic version of Dilacor XR been approved?


A generic version of Dilacor XR has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Dilacor XR and have been approved by the FDA:


diltiazem hydrochloride capsule, extended release; oral



  • Manufacturer: APOTEX

    Approval date: August 6, 1998

    Strength(s): 240MG [AB2]


  • Manufacturer: APOTEX

    Approval date: December 19, 2000

    Strength(s): 120MG [AB2], 180MG [AB2]


  • Manufacturer: MYLAN

    Approval date: March 18, 1998

    Strength(s): 120MG [AB2], 180MG [AB2], 240MG [AB2]


  • Manufacturer: WATSON LABS FLORIDA

    Approval date: October 10, 1997

    Strength(s): 120MG [AB2], 180MG [AB2], 240MG [AB2]

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




  • Tablets with controlled-rate release of active substances
    Patent 5,422,123
    Issued: June 6, 1995
    Inventor(s): Conte; Ubaldo & La Manna; Aldo & Colombo; Paolo
    Assignee(s): Jagotec AG
    Tablets with zero order controlled-rate of release of the active substances, consisting of a core of defined geometrical form containing the active substance, polymer substances which swell on contact with aqueous liquids and polymer substances with gelling properties, and a support applied to said core to partly cover its surface, the support consisting of polymer substances which are slowly soluble and/or slowly gellable in aqueous liquids, plasticizing substances, and possibly substances with an adjuvant function.
    Patent expiration dates:

    • June 6, 2012



See also...

  • Dilacor XR 24-Hour Sustained-Release Capsules Consumer Information (Wolters Kluwer)
  • Dilacor XR Consumer Information (Cerner Multum)
  • Dilacor XR Advanced Consumer Information (Micromedex)
  • Diltiazem Consumer Information (Drugs.com)
  • Diltiazem Consumer Information (Wolters Kluwer)
  • Diltiazem 12-Hour Sustained-Release Capsules Consumer Information (Wolters Kluwer)
  • Diltiazem 24-Hour Extended-Release Beads Capsules Consumer Information (Wolters Kluwer)
  • Diltiazem 24-Hour Extended-Release Beads Tablets Consumer Information (Wolters Kluwer)
  • Diltiazem 24-Hour Sustained-Release Beads Capsules Consumer Information (Wolters Kluwer)
  • Diltiazem 24-Hour Sustained-Release Capsules Consumer Information (Wolters Kluwer)
  • Diltiazem Immediate-Release Tablets Consumer Information (Wolters Kluwer)
  • Dilt-CD Consumer Information (Cerner Multum)
  • Diltiazem Consumer Information (Cerner Multum)
  • Dilt-CD Advanced Consumer Information (Micromedex)
  • Diltiazem Advanced Consumer Information (Micromedex)
  • Diltiazem Intravenous Advanced Consumer Information (Micromedex)
  • Diltiazem Hydrochloride AHFS DI Monographs (ASHP)