Thursday, September 22, 2016

Vosol HC


Vosol HC is a brand name of acetic acid/hydrocortisone otic, approved by the FDA in the following formulation(s):


VOSOL HC (acetic acid, glacial; hydrocortisone - solution/drops; otic)



  • Manufacturer: HI TECH PHARMA

    Approved Prior to Jan 1, 1982

    Strength(s): 2%;1% [RLD][AT]

Has a generic version of Vosol HC been approved?


Yes. The following products are equivalent to Vosol HC:


ACETASOL HC (acetic acid, glacial; hydrocortisone solution/drops; otic)



  • Manufacturer: ACTAVIS MID ATLANTIC

    Approval date: January 13, 1982

    Strength(s): 2%;1% [AT]

HYDROCORTISONE AND ACETIC ACID (acetic acid, glacial; hydrocortisone solution/drops; otic)



  • Manufacturer: TARO

    Approval date: March 4, 1985

    Strength(s): 2%;1% [AT]


  • Manufacturer: VINTAGE

    Approval date: February 6, 2006

    Strength(s): 2%;1% [AT]

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

See also...

  • Vosol HC Advanced Consumer Information (Micromedex)
  • Acetic Acid/Hydrocortisone Solution Consumer Information (Wolters Kluwer)
  • Acetic acid and hydrocortisone otic Consumer Information (Cerner Multum)
  • Hydrocortisone and acetic acid Otic Advanced Consumer Information (Micromedex)

Zyloprim


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


ZYLOPRIM (allopurinol - tablet; oral)



  • Manufacturer: PROMETHEUS LABS

    Approved Prior to Jan 1, 1982

    Strength(s): 100MG [AB], 300MG [RLD][AB]

Has a generic version of Zyloprim been approved?


Yes. The following products are equivalent to Zyloprim:


allopurinol tablet; oral



  • Manufacturer: APOTEX INC

    Approval date: September 8, 2005

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: CARACO

    Approval date: August 30, 2007

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: IPCA LABS LTD

    Approval date: March 16, 2011

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: MUTUAL PHARM

    Approval date: January 9, 1987

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: MYLAN

    Approval date: October 24, 1986

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: NORTHSTAR HLTHCARE

    Approval date: September 11, 2007

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: VINTAGE PHARMS

    Approval date: June 27, 2003

    Strength(s): 100MG [AB], 300MG [AB]


  • Manufacturer: WATSON LABS

    Approval date: September 28, 1984

    Strength(s): 100MG [AB], 300MG [AB]

LOPURIN (allopurinol tablet; oral)



  • Manufacturer: DR REDDYS LA

    Approval date: April 2, 1987

    Strength(s): 100MG [AB], 300MG [AB]

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

See also...

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

Valturna


Valturna is a brand name of aliskiren/valsartan, approved by the FDA in the following formulation(s):


VALTURNA (aliskiren hemifumarate; valsartan - tablet; oral)



  • Manufacturer: NOVARTIS

    Approval date: September 16, 2009

    Strength(s): EQ 150MG BASE;160MG, EQ 300MG BASE;320MG [RLD]

Has a generic version of Valturna been approved?


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


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




  • Acyl compounds
    Patent 5,399,578
    Issued: March 21, 1995
    Inventor(s): Buhlmayer; Peter & Ostermayer; Franz & Schmidlin; Tibur
    Assignee(s): Ciba-Geigy Corp
    Compounds of the formula ##STR1## in which R.sub.1 is an aliphatic hydrocarbon radical which is unsubstituted or substituted by halogen or hydroxyl, or a cycloaliphatic or araliphatic hydrocarbon radical; X.sub.1 is CO, SO.sub.2, or --O--C(.dbd.O)-- with the carbon atom of the carbonyl group being attached to the nitrogen atom shown in formula I; X.sub.2 is a divalent aliphatic hydrocarbon radical which is unsubstituted or substituted by hydroxyl, carboxyl, amino, guanidino or a cycloaliphatic or aromatic radical, or is a divalent cycloaliphatic hydrocarbon radical, it being possible for a carbon atom of the aliphatic hydrocarbon radical to be additionally bridged by a divalent aliphatic hydrocarbon radical; R.sub.2 is carboxyl which, if desired, is esterified or amidated, substituted or unsubstituted amino, formyl which, if desired, is acetalized, 1H-tetrazol-5-yl, pyridyl, hydroxyl which, if desired, is etherified, S(O).sub.m --R where m is 0, 1 or 2 and R is hydrogen or an aliphatic hydrocarbon radical, alkanoyl, unsubstituted or N-substituted sulfamoyl or PO.sub.n H.sub.2 where n is 2 or 3; X.sub.3 is a divalent aliphatic hydrocarbon; R.sub.3 is carboxyl, 5-tetrazolyl, SO.sub.3 H, PO.sub.2 H.sub.2, PO.sub.3 H.sub.2 or haloalkylsulfamoyl; and the rings A and B independently of one another are substituted or unsubstituted; in free form or in salt form, can be prepared in a manner known per se and can be used, for example, as medicament active ingredients.
    Patent expiration dates:

    • March 21, 2012
      ✓ 
      Patent use: TREATMENT OF HYPERTENSION
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • .delta.-amino-.gamma.-hydroxy-.omega.-aryl-alkanoic acid amides
    Patent 5,559,111
    Issued: September 24, 1996
    Inventor(s): G oschke; Richard & Maibaum; J urgen K. & Schilling; Walter & Stutz; Stefan & Rigollier; Pascal & Yamaguchi; Yasuchika & Cohen; Nissim C. & Herold; Peter
    Assignee(s): Ciba-Geigy Corporation
    .delta.-Amino-.gamma.-hydroxy-.omega.-aryl-alkanoic acid amides of formula I ##STR1## and the salts thereof, have renin-inhibiting properties and can be used as antihypertensive medicinal active ingredients.
    Patent expiration dates:

    • July 21, 2018
      ✓ 
      Patent use: TREATMENT OF HYPERTENSION
      ✓ 
      Drug substance
      ✓ 
      Drug product



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:
    • March 5, 2012 - NEW CHEMICAL ENTITY

    • September 16, 2012 - NEW COMBINATION

See also...

  • Valturna Consumer Information (Drugs.com)
  • Valturna Consumer Information (Wolters Kluwer)
  • Valturna Consumer Information (Cerner Multum)
  • Valturna Advanced Consumer Information (Micromedex)
  • Aliskiren/Valsartan Consumer Information (Wolters Kluwer)
  • Aliskiren and valsartan Consumer Information (Cerner Multum)
  • Aliskiren and valsartan Advanced Consumer Information (Micromedex)

Zebeta


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


ZEBETA (bisoprolol fumarate - tablet; oral)



  • Manufacturer: TEVA WOMENS

    Approval date: July 31, 1992

    Strength(s): 10MG [RLD][AB], 5MG [AB]

Has a generic version of Zebeta been approved?


Yes. The following products are equivalent to Zebeta:


bisoprolol fumarate tablet; oral



  • Manufacturer: AUROBINDO PHARMA

    Approval date: December 27, 2006

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: MYLAN

    Approval date: December 14, 2005

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: SANDOZ

    Approval date: November 16, 2000

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: TEVA PHARMS

    Approval date: June 26, 2001

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: UNICHEM PHARMS (USA)

    Approval date: August 18, 2009

    Strength(s): 10MG [AB], 5MG [AB]

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

See also...

  • Zebeta Consumer Information (Drugs.com)
  • Zebeta Consumer Information (Wolters Kluwer)
  • Zebeta Consumer Information (Cerner Multum)
  • Zebeta Advanced Consumer Information (Micromedex)
  • Zebeta AHFS DI Monographs (ASHP)
  • Bisoprolol Consumer Information (Drugs.com)
  • Bisoprolol Consumer Information (Wolters Kluwer)
  • Bisoprolol Consumer Information (Cerner Multum)
  • Bisoprolol Advanced Consumer Information (Micromedex)
  • Bisoprolol Fumarate AHFS DI Monographs (ASHP)

Faslodex


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


FASLODEX (fulvestrant - injectable; intramuscular)



  • Manufacturer: ASTRAZENECA

    Approval date: April 25, 2002

    Strength(s): 50MG/ML [RLD]

Has a generic version of Faslodex been approved?


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


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




  • Formulation
    Patent 6,774,122
    Issued: August 10, 2004
    Inventor(s): John R; Evans & Rosalind U; Grundy
    Assignee(s): AstraZeneca AB
    The invention relates to a novel sustained release pharmaceutical formulation adapted for administration by injection containing the compound 7&agr;-[9-(4,4,5,5,5-pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17&bgr;-diol, more particularly to a formulation adapted for administration by injection containing the compound 7&agr;-[9-(4,4,5,5,5-pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17&bgr;-diol in solution in a ricinoleate vehicle which additionally comprises at least one alcohol and a non-aqueous ester solvent which is miscible in the ricinoleate vehicle.
    Patent expiration dates:

    • January 9, 2021
      ✓ 
      Patent use: TREATMENT OF HORMONE RECEPTOR POSITIVE METASTATIC BREAST CANCER IN POSTMENOPAUSAL WOMEN WITH DISEASE PROGRESSION FOLLOWING ANTIESTROGEN THERAPY


    • July 9, 2021
      ✓ 
      Pediatric exclusivity




  • Formulation
    Patent 7,456,160
    Issued: November 25, 2008
    Inventor(s): Evans; John R & Grundy; Rosalind U
    Assignee(s): AstraZeneca AB
    The invention relates to a novel sustained release pharmaceutical formulation adapted for administration by injection containing the compound 7α-[9-(4,4,5,5,5-pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17β-diol, more particularly to a formulation adapted for administration by injection containing the compound 7α-[9-(4,4,5,5,5-pentafluoropentylsulphinyl)nonyl]oestra-1,3,5(10)-triene-3,17β-diol in solution in a ricinoleate vehicle which additionally comprises at least one alcohol and a non-aqueous ester solvent which is miscible in the ricinoleate vehicle.
    Patent expiration dates:

    • January 9, 2021
      ✓ 
      Patent use: TREATMENT OF HORMONE RECEPTOR POSITIVE METASTATIC BREAST CANCER IN POSTMENOPAUSAL WOMEN WITH DISEASE PROGRESSION FOLLOWING ANTIESTROGEN THERAPY


    • July 9, 2021
      ✓ 
      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:
    • September 9, 2013 - CHANGE DOSAGE REGIMEN FROM 250MG TO 500MG

    • March 9, 2014 - PEDIATRIC EXCLUSIVITY

    • May 17, 2014 - SAFETY, EFFICACY AND PHARMACOKINETIC INFO FOR FASLODEX IN THE PEDIATRIC POPULATION, SPECIFICALLY FOR GIRLS WITH PROGRESSIVE PRECOCIOUS PUBERTY ASSOCIATED WITH MCCUNE-ALBRIGHT SYNDROME ADDED TO THE PEDIATRIC USE SECTION OF THE LABELING

    • November 17, 2014 - PEDIATRIC EXCLUSIVITY

See also...

  • Faslodex Consumer Information (Drugs.com)
  • Faslodex Consumer Information (Wolters Kluwer)
  • Faslodex Consumer Information (Cerner Multum)
  • Faslodex Advanced Consumer Information (Micromedex)
  • Faslodex AHFS DI Monographs (ASHP)
  • Fulvestrant Consumer Information (Wolters Kluwer)
  • Fulvestrant Consumer Information (Cerner Multum)
  • Fulvestrant Intramuscular Advanced Consumer Information (Micromedex)
  • Fulvestrant AHFS DI Monographs (ASHP)

Zomig-ZMT


See also: Generic Zomig


Zomig-ZMT is a brand name of zolmitriptan, approved by the FDA in the following formulation(s):


ZOMIG-ZMT (zolmitriptan - tablet, orally disintegrating; oral)



  • Manufacturer: ASTRAZENECA

    Approval date: February 13, 2001

    Strength(s): 2.5MG


  • Manufacturer: ASTRAZENECA

    Approval date: September 17, 2001

    Strength(s): 5MG [RLD]

Has a generic version of Zomig-ZMT been approved?


No. There is currently no therapeutically equivalent version of Zomig-ZMT available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Zomig-ZMT. 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.




  • Indolyl compounds for treating migraine
    Patent 5,466,699
    Issued: November 14, 1995
    Inventor(s): Robertson; Alan D. & Hill; Alan P. & Glen; Robert C. & Martin; Graeme R.
    Assignee(s): Burroughs Wellcome Co.
    ##STR1## The present invention is concerned with compounds of formula (I), wherein n is an integer of from 0 to 3: W is a group of formula (i), (ii), or (iii), wherein R is hydrogen or C.sub.1-4 alkyl, X is --O--, --S--, --NH--, or --CH.sub.2 --, Y is oxygen or sulphur and the chiral center (*) in formula (i) or (ii) is in its (S) or (R) form or is a mixture thereof in any proportions: and Z is a group of formula (iv), (v), or (vi), wherein R.sup.1 and R.sup.2 are independently selected from hydrogen and C.sub.1-4 alkyl and R.sup.3 is hydrogen or C.sub.1-4 alkyl; and their salts, solvates and physiologically functional derivatives, with processes for their preparation, with medicaments containing them and with their use as therapeutic agents, particularly in the prophylaxis and treatment of migraine.
    Patent expiration dates:

    • November 14, 2012


    • May 14, 2013
      ✓ 
      Pediatric exclusivity



See also...

  • Zomig ZMT Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Zomig-ZMT Consumer Information (Cerner Multum)
  • Zomig-ZMT Advanced Consumer Information (Micromedex)
  • Zolmitriptan Consumer Information (Wolters Kluwer)
  • Zolmitriptan Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Zolmitriptan Spray Consumer Information (Wolters Kluwer)
  • Zolmitriptan Consumer Information (Cerner Multum)
  • Zolmitriptan nasal Consumer Information (Cerner Multum)
  • Zolmitriptan Advanced Consumer Information (Micromedex)
  • Zolmitriptan AHFS DI Monographs (ASHP)

Zolpimist


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


ZOLPIMIST (zolpidem tartrate - spray, metered; oral)



  • Manufacturer: NOVADEL

    Approval date: December 19, 2008

    Strength(s): 5MG/SPRAY [RLD]

Has a generic version of Zolpimist been approved?


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


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




  • Buccal, polar and non-polar spray containing zolpidem
    Patent 7,632,517
    Issued: December 15, 2009
    Inventor(s): Dugger, III; Harry A. & Abd El-Shafy; Mohammed
    Assignee(s): Novadel Pharma Inc.
    Buccal aerosol sprays or capsules using polar and non-polar solvents have now been developed which provide zolpidem for rapid absorption through the oral mucosa, resulting in fast onset of effect. The buccal polar compositions of the invention comprise formulation I: aqueous polar solvent, zolpidem, and optional flavoring agent; formulation II: aqueous polar solvent, zolpidem, optionally flavoring agent, and propellant; formulation III: non-polar solvent, zolpidem, and optional flavoring agent; formulation IV: non-polar solvent, zolpidem, optional flavoring agent, and propellant; formulation V: a mixture of a polar solvent and a non-polar solvent, zolpidem, and optional flavoring agent; formulation VI: a mixture of a polar solvent and a non-polar solvent, zolpidem, optional flavoring agent, and propellant.
    Patent expiration dates:

    • October 1, 2017
      ✓ 
      Patent use: TREATMENT OF TRANSIENT INSOMNIA



See also...

  • ZolpiMist Consumer Information (Drugs.com)
  • Zolpimist Oral Spray Consumer Information (Wolters Kluwer)
  • Zolpimist Consumer Information (Cerner Multum)
  • Zolpimist Advanced Consumer Information (Micromedex)
  • Zolpidem Consumer Information (Drugs.com)
  • Zolpidem Consumer Information (Wolters Kluwer)
  • Zolpidem Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Zolpidem Oral Spray Consumer Information (Wolters Kluwer)
  • Zolpidem Consumer Information (Cerner Multum)
  • Zolpidem Oral, Oromucosal Advanced Consumer Information (Micromedex)
  • Zolpidem Tartrate AHFS DI Monographs (ASHP)