Monday, October 24, 2016

Luveris


Luveris is a brand name of lutropin alfa, approved by the FDA in the following formulation(s):


LUVERIS (lutropin alfa - injectable; subcutaneous)



  • Manufacturer: EMD SERONO

    Approval date: October 8, 2004

    Strength(s): 75 IU/VIAL [RLD]

Has a generic version of Luveris been approved?


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


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




  • Recombinant heterodimeric human fertility hormones, and methods, cells, and vectors and DNA for the production thereof
    Patent 5,767,251
    Issued: June 16, 1998
    Inventor(s): Reddy; Vermuri B. & Hsiung; Nancy & Beck; Anton K. & Bernstine; Edward George
    Assignee(s): Genzyme Corporation
    Biologically active heterodimeric human fertility hormones composed of two different subunits, each subunit being synthesized in the same cell transformed by at least one cell expression vector having heterologous DNA encoding each subunit with each subunit being controlled by a separate promoter. Preferred human fertility hormones include hCG, hLH and hFSH.
    Patent expiration dates:

    • June 16, 2015
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      Drug substance



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:
    • October 8, 2011 - ORPHAN DRUG EXCLUSIVITY

See also...

  • Luveris Consumer Information (Drugs.com)
  • Luveris Consumer Information (Wolters Kluwer)
  • Luveris Consumer Information (Cerner Multum)
  • Luveris Advanced Consumer Information (Micromedex)
  • Luveris AHFS DI Monographs (ASHP)
  • Lutropin Alfa Consumer Information (Wolters Kluwer)
  • Lutropin alfa Consumer Information (Cerner Multum)
  • Lutropin alfa Subcutaneous Advanced Consumer Information (Micromedex)
  • Lutropin Alfa AHFS DI Monographs (ASHP)

Lovaza


Lovaza is a brand name of omega-3 polyunsaturated fatty acids, approved by the FDA in the following formulation(s):


LOVAZA (omega-3-acid ethyl esters - capsule; oral)



  • Manufacturer: SMITHKLINE BEECHAM

    Approval date: November 10, 2004

    Strength(s): 1GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS [RLD]

Has a generic version of Lovaza been approved?


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


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




  • Fatty acid composition
    Patent 5,502,077
    Issued: March 26, 1996
    Inventor(s): Breivik; Harald & Borretzen; Bernt & Dahl; Knut H. & Krokan; Hans E. & Bonaa; Kaare H.
    Assignee(s): Norsk Hydro A.S.
    Fatty acid composition comprising at least 80% by weight of omega-3-fatty acids, salts or derivatives thereof, wherein (all-Z)-5,8,11,14,17-eicosapentaenoic acid (EPA) and (all-Z)-4,7,10,13,16,19-docosahexaenoic acid comprises at least 75% by weight of the total fatty acids. The compositions can be used for the treatment or prophylaxis of multiple risk factors for cardiovascular diseases.
    Patent expiration dates:

    • March 26, 2013
      ✓ 
      Patent use: USE IN LIPID MANAGEMENT
      ✓ 
      Drug substance




  • Fatty acid composition
    Patent 5,656,667
    Issued: August 12, 1997
    Inventor(s): Breivik; Harald & B.o slashed.rretzen; Bernt & Dahl; Knut Helk.ang.s & Krokan; Hans Einar & B.o slashed.naa; Kaare Harald
    Assignee(s): Norsk Hydro as
    Fatty acid composition comprising at least 80% by weight of omega-3-fatty acids, salts or derivatives thereof, wherein (all-Z)-5,8,11,14,17-eicosapentaenoic acid (EPA) and (all-Z)-4,7,10,13,16,19-docosahexaenoic acid comprises at least 75% by weight of the total fatty acids. The compositions can be used for the treatment or prophylaxis of multiple risk factors for cardiovascular diseases.
    Patent expiration dates:

    • April 10, 2017
      ✓ 
      Patent use: USE IN LIPID MANAGEMENT
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Pharmaceutical composition comprising low concentrations of environmental pollutants
    Patent 7,732,488
    Issued: June 8, 2010
    Inventor(s): Breivik; Harald & Thorstad; Olav
    Assignee(s): Pronova Biopharma Norge AS
    The invention relates to a process for decreasing the amount of environmental pollutants in a mixture comprising a fat or an oil, being edible or for use in cosmetics, the fat or oil containing the environmental pollutants, which process comprises the steps of adding a volatile working fluid to the mixture, where the volatile working fluid comprises at least one of a fatty acid ester, a fatty acid amide, a free fatty acid and a hydro-carbon, and subjecting the mixture with the added volatile working fluid to at least one stripping processing step, in which an amount of environmental pollutant present in the fat or oil, being edible or for use in cosmetics, is separated from the mixture together with the volatile working fluid. The present invention also relates to a volatile environmental pollutants decreasing working fluid, for use in decreasing an amount of environmental pollutants present in a fat or oil, being edible or for use in cosmetics. In addition, the present invention relates to a health supplement, a pharmaceutical and an animal feed product prepared according to the process mentioned above.
    Patent expiration dates:

    • January 30, 2025
      ✓ 
      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:
    • September 16, 2012 - INCLUSION OF RESULTS FROM TWO DRUG INTERACTION STUDIES WITH LIPITOR AND CRESTOR IN CLINICAL PHARMACOLOGY SECTION

See also...

  • Lovaza Consumer Information (Wolters Kluwer)
  • Lovaza Consumer Information (Cerner Multum)
  • Lovaza Advanced Consumer Information (Micromedex)
  • Folic Acid/Vitamin B6/Vitamin B12/Omega-3 Acids/Phytosterols Consumer Information (Wolters Kluwer)
  • Folic Acid/Vitamin B6/Vitamin B12/Omega-3 Fatty Acids/Biotin/Chromium Consumer Information (Wolters Kluwer)
  • Omega-3-Acid Ethyl Esters Consumer Information (Wolters Kluwer)
  • Omega-3 polyunsaturated fatty acids Consumer Information (Cerner Multum)
  • Omega-3-acid ethyl esters Advanced Consumer Information (Micromedex)
  • Omega-3-acid Ethyl Esters AHFS DI Monographs (ASHP)
  • Fish Oils Natural Product Information (Facts & Comparisons)

LoSeasonique


LoSeasonique is a brand name of ethinyl estradiol/levonorgestrel, approved by the FDA in the following formulation(s):


LOSEASONIQUE (ethinyl estradiol; levonorgestrel - tablet; oral)



  • Manufacturer: TEVA WOMENS

    Approval date: October 24, 2008

    Strength(s): 0.02MG,0.01MG;0.1MG,N/A [AB]

Has a generic version of LoSeasonique been approved?


A generic version of LoSeasonique 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 LoSeasonique and have been approved by the FDA:


LEVONORGESTREL AND ETHINYL ESTRADIOL (ethinyl estradiol; levonorgestrel tablet; oral)



  • Manufacturer: LUPIN LTD

    Approval date: October 26, 2011

    Strength(s): 0.02MG,0.01MG;0.1MG,N/A [AB]


  • Manufacturer: WATSON LABS

    Approval date: October 25, 2011

    Strength(s): 0.02MG,0.01MG;0.1MG,N/A [AB]

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




  • Oral contraceptives to prevent pregnancy and diminish premenstrual symptomatology
    Patent 7,615,545
    Issued: November 10, 2009
    Inventor(s): Bell; Robert G. & Ben-Maimon; Carole & Iskold; Beata
    Assignee(s): Duramed Pharmaceuticals, Inc.
    This invention relates to a method of preventing pregnancy and treating PMS including PMDD. More particularly, the invention relates to a method, which involves administering one of several combination oral contraceptive regimens in combination with an antidepressant and a kit containing the same.
    Patent expiration dates:

    • June 15, 2023
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      Patent use: PREVENTION OF PREGNANCY




  • Methods of hormonal treatment utilizing contraceptive regimens with continuous estrogen administration
    Patent 7,855,190
    Issued: December 21, 2010
    Inventor(s): Bell; Robert G. & Ben-Maimon; Carole S. & Iskold; Beata & Bronnenkant; Lance J. & Hait; Howard & Reape; Kathleen Z.
    Assignee(s): Teva Women's Health, Inc.
    The present invention provides contraceptive regimens in which a female is administered a combined dosage form of estrogen and progestin followed by a period of administration of estrogen. The disclosed contraceptive regimens can be administered to a female as a method of providing non-contraceptive benefits.
    Patent expiration dates:

    • December 5, 2028
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      Patent use: PREVENTION OF PREGNANCY




  • Oral contraceptives to prevent pregnancy and diminish premenstrual symptomatology
    Patent 7,858,605
    Issued: December 28, 2010
    Inventor(s): Bell; Robert G. & Ben-Maimon; Carole & Iskold; Beata
    Assignee(s): Teva Women's Health, Inc.
    This invention relates to a method of preventing pregnancy and treating PMS including PMDD. More particularly, the invention relates to a method, which involves administering one of several combination oral contraceptive regimens in combination with an antidepressant and a kit containing the same.
    Patent expiration dates:

    • June 23, 2023
      ✓ 
      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:
    • October 24, 2011 - NEW PRODUCT

See also...

  • LoSeasonique Consumer Information (Drugs.com)
  • LoSeasonique Consumer Information (Wolters Kluwer)
  • LoSeasonique extended-cycle Consumer Information (Cerner Multum)
  • Levonorgestrel/Ethinyl Estradiol Consumer Information (Wolters Kluwer)
  • Ethinyl estradiol and levonorgestrel Consumer Information (Cerner Multum)
  • Ethinyl estradiol and levonorgestrel extended-cycle Consumer Information (Cerner Multum)

Lybrel


Lybrel is a brand name of ethinyl estradiol/levonorgestrel, approved by the FDA in the following formulation(s):


LYBREL (ethinyl estradiol; levonorgestrel - tablet; oral)



  • Manufacturer: WYETH PHARMS INC

    Approval date: May 22, 2007

    Strength(s): 0.02MG;0.09MG [RLD][AB]

Has a generic version of Lybrel been approved?


A generic version of Lybrel 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 Lybrel and have been approved by the FDA:


LEVONORGESTREL AND ETHINYL ESTRADIOL (ethinyl estradiol; levonorgestrel tablet; oral)



  • Manufacturer: WATSON LABS

    Approval date: June 6, 2011

    Strength(s): 0.02MG;0.09MG [AB]

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




  • Hormonal contraceptive
    Patent 6,500,814
    Issued: December 31, 2002
    Inventor(s): Rolf-Dieter; Hesch
    Assignee(s): Wyeth Pharmaceuticals
    The present invention relates to a hormonal contraceptive product having two hormonal components, an estrogen and a gestagen, and a process for the combined, continuous administration of the product of the invention.
    Patent expiration dates:

    • September 3, 2018
      ✓ 
      Patent use: PREVENTION OF PREGNANCY



See also...

  • Lybrel Consumer Information (Drugs.com)
  • Lybrel Consumer Information (Wolters Kluwer)
  • Lybrel Consumer Information (Cerner Multum)
  • Levonorgestrel/Ethinyl Estradiol Consumer Information (Wolters Kluwer)
  • Ethinyl estradiol and levonorgestrel Consumer Information (Cerner Multum)
  • Ethinyl estradiol and levonorgestrel extended-cycle Consumer Information (Cerner Multum)

Restoril


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


RESTORIL (temazepam - capsule; oral)



  • Manufacturer: MALLINCKRODT INC

    Approved Prior to Jan 1, 1982

    Strength(s): 15MG [AB], 30MG [RLD][AB]


  • Manufacturer: MALLINCKRODT INC

    Approval date: October 25, 1991

    Strength(s): 7.5MG [AB]


  • Manufacturer: MALLINCKRODT INC

    Approval date: November 2, 2004

    Strength(s): 22.5MG [AB]

Has a generic version of Restoril been approved?


Yes. The following products are equivalent to Restoril:


temazepam capsule; oral



  • Manufacturer: ACTAVIS ELIZABETH

    Approval date: August 7, 1987

    Strength(s): 15MG [AB], 30MG [AB]


  • Manufacturer: MUTUAL PHARM

    Approval date: September 8, 2009

    Strength(s): 7.5MG [AB]


  • Manufacturer: MUTUAL PHARM

    Approval date: September 14, 2009

    Strength(s): 22.5MG [AB]


  • Manufacturer: MYLAN

    Approval date: July 7, 1986

    Strength(s): 15MG [AB]


  • Manufacturer: MYLAN

    Approval date: July 10, 1986

    Strength(s): 30MG [AB]


  • Manufacturer: MYLAN

    Approval date: June 12, 2009

    Strength(s): 22.5MG [AB]


  • Manufacturer: MYLAN

    Approval date: May 21, 2010

    Strength(s): 7.5MG [AB]


  • Manufacturer: NOVEL LABS INC

    Approval date: April 21, 1987

    Strength(s): 15MG [AB], 30MG [AB]


  • Manufacturer: SANDOZ

    Approval date: January 12, 1988

    Strength(s): 15MG [AB], 30MG [AB]


  • Manufacturer: WATSON LABS

    Approval date: May 21, 1993

    Strength(s): 15MG [AB], 30MG [AB]

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

See also...

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

Azor


Azor is a brand name of amlodipine/olmesartan, approved by the FDA in the following formulation(s):


AZOR (amlodipine besylate; olmesartan medoxomil - tablet; oral)



  • Manufacturer: DAIICHI SANKYO

    Approval date: September 26, 2007

    Strength(s): EQ 10MG BASE;20MG, EQ 10MG BASE;40MG [RLD], EQ 5MG BASE;20MG, EQ 5MG BASE;40MG

Has a generic version of Azor been approved?


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


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




  • Angiotensin II antagosist 1-biphenylmethylimidazole compounds and their therapeutic use
    Patent 5,616,599
    Issued: April 1, 1997
    Inventor(s): Yanagisawa; Hiroaki & Fujimoto; Koichi & Amemiya; Yoshiya & Shimoji; Yasuo & Kanazaki; Takuro & Koike; Hiroyuki & Sada; Toshio
    Assignee(s): Sankyo Company, Limited
    Compounds of the following formula (I) or the formula (I).sub.p : ##STR1## wherein R.sup.1 is alkyl or alkenyl; R.sup.2 and R.sup.3 are hydrogen, alkyl, alkenyl, cycloalkyl, aralkyl, aryl, or aryl fused to cycloalkyl; R.sup.4 is hydrogen, alkyl, alkanoyl, alkenoyl, arylcarbonyl, alkoxycarbonyl, tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydrothienyl, tetrahydrofuryl, a group of formula --SiR.sup.a R.sup.b R.sup.c, in which R.sup.a, R.sup.b and R.sup.c are alkyl or aryl, alkoxymethyl, (alkoxyalkoxy)methyl, haloalkoxymethyl, aralkyl, aryl or alkanoyloxymethoxycarbonyl; R.sup.5 is carboxy or --CONR.sup.8 R.sup.9, wherein R.sup.8 and R.sup.9 hydrogens or alkyl, or R.sup.8 and R.sup.9 together form alkylene; R.sup.6 is hydrogen, alkyl, alkoxy or halogen; R.sup.7 is carboxy or tetrazol-5-yl; R.sub.p.sup.1 is hydrogen, alkyl, cycloalkyl or alkanoyl; R.sub.p.sup.2 is a single bond, alkylene or alkylidene; R.sub.p.sup.3 and R.sub.p.sup.4 are each hydrogen or alkyl; R.sub.p.sup.6 is carboxy or tetrazol-5-yl; and X.sub.p is oxygen or sulfur; and pharmaceutically acceptable salts and esters thereof. The compounds are AII receptor antagonists and thus have hypotensive activity and can be used for the treatment and prophylaxis of hypertension. The compounds may be prepared by reacting a biphenylmethyl compound with an imidazole compound.
    Patent expiration dates:

    • April 25, 2016
      ✓ 
      Patent use: TREATMENT OF HYPERTENSION
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • October 25, 2016
      ✓ 
      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 26, 2010 - NEW COMBINATION

See also...

  • Azor Consumer Information (Drugs.com)
  • Azor Consumer Information (Wolters Kluwer)
  • Azor Consumer Information (Cerner Multum)
  • Azor Advanced Consumer Information (Micromedex)
  • Amlodipine/Olmesartan Consumer Information (Wolters Kluwer)
  • Amlodipine and olmesartan Consumer Information (Cerner Multum)
  • Amlodipine and olmesartan Advanced Consumer Information (Micromedex)

Differin


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


DIFFERIN (adapalene - cream; topical)



  • Manufacturer: GALDERMA LABS LP

    Approval date: May 26, 2000

    Strength(s): 0.1% [RLD][AB]

DIFFERIN (adapalene - gel; topical)



  • Manufacturer: GALDERMA LABS LP

    Approval date: May 31, 1996

    Strength(s): 0.1% [RLD][AB]


  • Manufacturer: GALDERMA LABS LP

    Approval date: June 19, 2007

    Strength(s): 0.3% [RLD]

DIFFERIN (adapalene - lotion; topical)



  • Manufacturer: GALDERMA R AND D

    Approval date: March 17, 2010

    Strength(s): 0.1% [RLD]

Has a generic version of Differin been approved?


A generic version of Differin 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 Differin and have been approved by the FDA:


adapalene cream; topical



  • Manufacturer: FOUGERA PHARMS

    Approval date: June 30, 2010

    Strength(s): 0.1% [AB]

adapalene gel; topical



  • Manufacturer: GLENMARK GENERICS

    Approval date: July 1, 2010

    Strength(s): 0.1% [AB]


  • Manufacturer: PLIVA HRVATSKA DOO

    Approval date: June 2, 2010

    Strength(s): 0.1% [AB]

Note: No generic formulation of the following product is available.


  • adapalene - lotion; topical

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




  • Administration of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid for the treatment of dermatological disorders
    Patent 7,579,377
    Issued: August 25, 2009
    Inventor(s): Graeber; Michael & Czernielewski; Janusz
    Assignee(s): Galderma Research & Development
    Dermatological disorders having an inflammatory or proliferative component are treated with pharmaceutical compositions containing on the order of 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthanoic acid (adapalene) or salt thereof, formulated into pharmaceutically acceptable media therefore, advantageously topically applicable gels, creams or lotions.
    Patent expiration dates:

    • February 23, 2025
      ✓ 
      Patent use: TOPICAL TREATMENT OF ACNE VULGARIS




  • Pharmaceutical compositions comprising 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid for the treatment of dermatological disorders
    Patent 7,737,181
    Issued: June 15, 2010
    Inventor(s): Graeber; Michael & Czernielewski; Janusz
    Assignee(s): Galderma Research & Development
    Dermatological disorders having an inflammatory or proliferative component, notably common acne, are treated with topically applicable pharmaceutical compositions containing about 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthanoic acid (adapalene) or salt thereof, formulated into pharmaceutically acceptable media therefor, advantageously formulated into topically applicable gels, preferably aqueous gels, creams, lotions or solutions.
    Patent expiration dates:

    • August 29, 2024
      ✓ 
      Drug product




  • Administration of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphtoic acid for the treatment of dermatological disorders
    Patent 7,834,060
    Issued: November 16, 2010
    Inventor(s): Graeber; Michael & Czernielewski; Janusz
    Assignee(s): Galderma Research & Development
    Dermatological disorders having an inflammatory or proliferative component are treated with pharmaceutical compositions containing on the order of 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthanoic acid (adapalene) or salt thereof, formulated into pharmaceutically acceptable media therefor, advantageously topically applicable gels, creams or lotions.
    Patent expiration dates:

    • March 12, 2023
      ✓ 
      Patent use: TREATMENT OF ACNE




  • Administration of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid for the treatment of dermatological disorders
    Patent 7,838,558
    Issued: November 23, 2010
    Inventor(s): Graeber; Michael & Czernielewski; Janusz
    Assignee(s): Galderma Research & Development S.N.C.
    Dermatological disorders having an inflammatory or proliferative component are treated with pharmaceutical compositions containing on the order of 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthanoic acid (adapalene) or salt thereof, formulated into pharmaceutically acceptable media therefor, advantageously topically applicable gels, creams or lotions.
    Patent expiration dates:

    • March 12, 2023
      ✓ 
      Drug product




  • Method for the treatment of acne using compositions comprising 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid
    Patent 7,868,044
    Issued: January 11, 2011
    Inventor(s): Graeber; Michael & Czernielewski; Janusz
    Assignee(s): Galderma Research & Development
    Dermatological disorders having an inflammatory or proliferative component, notably common acne, are treated with topically applicable pharmaceutical compositions containing about 0.3% by weight of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthanoic acid (adapalene) or salt thereof, formulated into pharmaceutically acceptable media therefor, advantageously formulated into topically applicable gels, preferably aqueous gels, creams, lotions or solutions.
    Patent expiration dates:

    • March 12, 2023
      ✓ 
      Patent use: TREATMENT OF ACNE




  • Cosmetic/dermatological compositions comprising naphthoic acid compounds and polyurethane polymers
    Patent 7,998,467
    Issued: August 16, 2011
    Inventor(s): Mallard; Claire & Ferrara; Eve
    Assignee(s): Galderma Research & Development
    Cosmetic/dermatological compositions for topical application and useful for the treatment, e.g., of acne, contain, formulated into a physiologically acceptable medium, at least one naphthoic acid compound and at least one polyurethane polymer or derivative thereof, the at least one naphthoic acid compound being dispersed therein.
    Patent expiration dates:

    • May 31, 2028
      ✓ 
      Patent use: TREATMENT OF ACNE
      ✓ 
      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 17, 2013 - NEW DOSAGE FORM

See also...

  • Differin Consumer Information (Drugs.com)
  • Differin Cream Consumer Information (Wolters Kluwer)
  • Differin Lotion Consumer Information (Wolters Kluwer)
  • Differin Pads Consumer Information (Wolters Kluwer)
  • Differin Solution Consumer Information (Wolters Kluwer)
  • Differin Consumer Information (Cerner Multum)
  • Differin Topical Advanced Consumer Information (Micromedex)
  • Differin AHFS DI Monographs (ASHP)
  • Adapalene Cream Consumer Information (Wolters Kluwer)
  • Adapalene Lotion Consumer Information (Wolters Kluwer)
  • Adapalene Pads Consumer Information (Wolters Kluwer)
  • Adapalene Solution Consumer Information (Wolters Kluwer)
  • Adapalene topical Consumer Information (Cerner Multum)
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