Thursday, September 29, 2016

Spanil




Spanil may be available in the countries listed below.


Ingredient matches for Spanil



Scopolamine

Scopolamine is reported as an ingredient of Spanil in the following countries:


  • Bangladesh

International Drug Name Search

Acanya


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


ACANYA (benzoyl peroxide; clindamycin phosphate - gel; topical)



  • Manufacturer: DOW PHARM SCI

    Approval date: October 23, 2008

    Strength(s): 2.5%;1.2% [RLD]

Has a generic version of Acanya been approved?


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


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




  • Compositions of clindamycin and benzoyl peroxide for acne treatment
    Patent 5,733,886
    Issued: March 31, 1998
    Inventor(s): Baroody; Lloyd J. & Dow; Gordon J. & Dow; Debra A. & Lathrop; Robert
    Assignee(s): Baroody; Lloyd J.
    Dow; Gordon J.
    Compositions suitable for the treatment of acne by topical application comprise clindamycin and benzoyl peroxide. Kits for preparing the compositions include a solution of clindamycin in a first container and a gel suspension of benzoyl peroxide in a second container. Each component is stored at a pH which promotes stability, and the combination of the two components provides a final composition having a pH which promotes stability and enhances viscosity.
    Patent expiration dates:

    • March 31, 2015
      ✓ 
      Patent use: TREATMENT OF ACNE
      ✓ 
      Drug product




  • Compositions for the treatment of acne containing clindamycin and benzoyl peroxide
    Patent 6,117,843
    Issued: September 12, 2000
    Inventor(s): Baroody; Lloyd J. & Dow; Gordon J. & Dow; Debra A. & Lathrop; Robert
    Assignee(s): Baroody; Lloyd J.
    Dow; Gordon J.
    A pharmaceutical composition containing clindamycin and benzoyl peroxide is disclosed for the treatment of acne. The composition is stable for several months when stored at room temperature. Methods of preparing and of using the composition are disclosed.
    Patent expiration dates:

    • February 18, 2012
      ✓ 
      Drug product



See also...

  • Acanya Consumer Information (Drugs.com)
  • Acanya Gel Consumer Information (Wolters Kluwer)
  • Acanya Consumer Information (Cerner Multum)
  • Clindamycin/Benzoyl Peroxide Gel Consumer Information (Wolters Kluwer)
  • Benzoyl peroxide and clindamycin topical Consumer Information (Cerner Multum)
  • Clindoxyl Advanced Consumer Information (Micromedex)
  • Benzoyl peroxide and clindamycin Topical application Advanced Consumer Information (Micromedex)

Wednesday, September 28, 2016

Sinemet


See also: Generic Sinemet CR


Sinemet is a brand name of carbidopa/levodopa, approved by the FDA in the following formulation(s):


SINEMET (carbidopa; levodopa - tablet; oral)



  • Manufacturer: MERCK SHARP DOHME

    Approved Prior to Jan 1, 1982

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [RLD][AB]

Has a generic version of Sinemet been approved?


Yes. The following products are equivalent to Sinemet:


CARBIDOPA AND LEVODOPA (carbidopa; levodopa tablet; oral)



  • Manufacturer: ACTAVIS ELIZABETH

    Approval date: September 3, 1993

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [AB]


  • Manufacturer: APOTEX INC

    Approval date: June 2, 2008

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [AB]


  • Manufacturer: MYLAN

    Approval date: September 28, 2009

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [AB]


  • Manufacturer: SUN PHARM INDS

    Approval date: October 28, 2008

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [AB]


  • Manufacturer: TEVA

    Approval date: August 28, 1992

    Strength(s): 10MG;100MG [AB], 25MG;100MG [AB], 25MG;250MG [AB]

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

See also...

  • Sinemet Consumer Information (Wolters Kluwer)
  • Sinemet Consumer Information (Cerner Multum)
  • Carbidopa/Levodopa Consumer Information (Wolters Kluwer)
  • Carbidopa/Levodopa Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Carbidopa/Levodopa Sustained-Release Tablets Consumer Information (Wolters Kluwer)
  • Carbidopa and levodopa Consumer Information (Cerner Multum)
  • Levodopa/Carbidopa AHFS DI Monographs (ASHP)
  • Lodosyn AHFS DI Monographs (ASHP)

Sinemet CR


See also: Generic Sinemet


Sinemet CR is a brand name of carbidopa/levodopa, approved by the FDA in the following formulation(s):


SINEMET CR (carbidopa; levodopa - tablet, extended release; oral)



  • Manufacturer: MERCK SHARP DOHME

    Approval date: May 30, 1991

    Strength(s): 50MG;200MG [RLD][AB]


  • Manufacturer: MERCK SHARP DOHME

    Approval date: December 24, 1992

    Strength(s): 25MG;100MG [AB]

Has a generic version of Sinemet CR been approved?


Yes. The following products are equivalent to Sinemet CR:


CARBIDOPA AND LEVODOPA (carbidopa; levodopa tablet, extended release; oral)



  • Manufacturer: APOTEX

    Approval date: June 16, 2004

    Strength(s): 25MG;100MG [AB], 50MG;200MG [AB]


  • Manufacturer: IMPAX LABS

    Approval date: May 14, 2004

    Strength(s): 25MG;100MG [AB], 50MG;200MG [AB]


  • Manufacturer: MYLAN

    Approval date: September 30, 1999

    Strength(s): 50MG;200MG [AB]


  • Manufacturer: MYLAN

    Approval date: April 21, 2000

    Strength(s): 25MG;100MG [AB]


  • Manufacturer: SUN PHARM INDS

    Approval date: August 23, 2007

    Strength(s): 25MG;100MG [AB], 50MG;200MG [AB]

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

See also...

  • Sinemet CR Sustained-Release Tablets Consumer Information (Wolters Kluwer)
  • Sinemet CR Consumer Information (Cerner Multum)
  • Carbidopa/Levodopa Consumer Information (Wolters Kluwer)
  • Carbidopa/Levodopa Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Carbidopa/Levodopa Sustained-Release Tablets Consumer Information (Wolters Kluwer)
  • Carbidopa and levodopa Consumer Information (Cerner Multum)
  • Levodopa/Carbidopa AHFS DI Monographs (ASHP)
  • Lodosyn AHFS DI Monographs (ASHP)

Solodyn


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


SOLODYN (minocycline hydrochloride - tablet, extended release; oral)



  • Manufacturer: MEDICIS

    Approval date: May 8, 2006

    Strength(s): EQ 135MG BASE [RLD][AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]


  • Manufacturer: MEDICIS

    Approval date: July 23, 2009

    Strength(s): EQ 115MG BASE, EQ 65MG BASE


  • Manufacturer: MEDICIS

    Approval date: August 27, 2010

    Strength(s): EQ 105MG BASE, EQ 55MG BASE, EQ 80MG BASE

Has a generic version of Solodyn been approved?


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


minocycline hydrochloride tablet, extended release; oral



  • Manufacturer: BARR

    Approval date: March 17, 2009

    Strength(s): EQ 135MG BASE [AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]


  • Manufacturer: IMPAX LABS INC

    Approval date: February 3, 2009

    Strength(s): EQ 135MG BASE [AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]


  • Manufacturer: LUPIN LTD

    Approval date: November 30, 2011

    Strength(s): EQ 135MG BASE [AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]


  • Manufacturer: MATRIX LABS LTD

    Approval date: July 20, 2010

    Strength(s): EQ 135MG BASE [AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]


  • Manufacturer: SANDOZ

    Approval date: August 13, 2009

    Strength(s): EQ 135MG BASE [AB], EQ 45MG BASE [AB], EQ 90MG BASE [AB]

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




  • Method for the treatment of acne
    Patent 5,908,838
    Issued: June 1, 1999
    Inventor(s): Gans; Eugene H.
    Assignee(s): Medics Pharmaceutical Corporation
    A method for the treatment of acne is provided which results in the reduction of vestibular side effects following administration of oral tetracycline antibiotics.
    Patent expiration dates:

    • February 19, 2018
      ✓ 
      Patent use: TREATMENT OF INFLAMMATORY LESIONS OF NON-NODULAR MODERATE TO SEVERE ACNE VULGARIS




  • Minocycline oral dosage forms for the treatment of acne
    Patent 7,541,347
    Issued: June 2, 2009
    Inventor(s): Wortzman; Mitchell & Plott; R. Todd & Bhatia; Kuljit & Patel; Bhiku
    Assignee(s): Medicis Pharmaceutical Coropration
    Minocycline oral dosage forms containing a controlled release carrier are useful for the treatment of acne.
    Patent expiration dates:

    • April 2, 2027
      ✓ 
      Patent use: TREATMENT OF INFLAMMATORY LESIONS OF NON-NODULAR MODERATE TO SEVERE ACNE VULGARIS




  • Minocycline oral dosage forms for the treatment of acne
    Patent 7,544,373
    Issued: June 9, 2009
    Inventor(s): Wortzman; Mitchell & Plott; R. Todd & Bhatia; Kuljit & Patel; Bhiku
    Assignee(s): Medicis Pharmaceutical Corporation
    Minocycline oral dosage forms containing a controlled release carrier are useful for the treatment of acne.
    Patent expiration dates:

    • April 2, 2027
      ✓ 
      Drug product




  • Minocycline oral dosage forms for the treatment of acne
    Patent 7,790,705
    Issued: September 7, 2010
    Inventor(s): Wortzman; Mitchell & Plott; R. Todd & Bhatia; Kuljit & Patel; Bhiku
    Assignee(s): Medicis Pharmaceutical Corporation
    Minocycline oral dosage forms containing a controlled release carrier are useful for the treatment of acne.
    Patent expiration dates:

    • June 24, 2025
      ✓ 
      Patent use: TREATMENT OF ACNE




  • Method for the treatment of acne
    Patent 7,919,483
    Issued: April 5, 2011
    Inventor(s): Wortzman; Mitchell & Plott; R. Todd & Bhatia; Kuljit & Patel; Bhiku
    Assignee(s): Medicis Pharmaceutical Corporation
    A method for treatment of acne with tetracyclines is provided. A lower sustained dose and no loading dose is employed, with an optional once-a-day dosing regimen.
    Patent expiration dates:

    • March 7, 2027
      ✓ 
      Patent use: TREATMENT OF ACNE



See also...

  • Solodyn Consumer Information (Drugs.com)
  • Solodyn Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Solodyn Consumer Information (Cerner Multum)
  • Minocycline Consumer Information (Drugs.com)
  • Minocycline Consumer Information (Wolters Kluwer)
  • Minocycline Capsules Consumer Information (Wolters Kluwer)
  • Minocycline Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Minocycline Injection Consumer Information (Wolters Kluwer)
  • Minocycline Pellet-Filled Capsules Consumer Information (Wolters Kluwer)
  • Minocycline Consumer Information (Cerner Multum)
  • Arestin eent AHFS DI Monographs (ASHP)
  • Minocycline Hydrochloride AHFS DI Monographs (ASHP)
  • Minocycline Hydrochloride eent AHFS DI Monographs (ASHP)

Procid




Procid may be available in the countries listed below.


Ingredient matches for Procid



Omeprazole

Omeprazole is reported as an ingredient of Procid in the following countries:


  • India

Probenecid

Probenecid is reported as an ingredient of Procid in the following countries:


  • Taiwan

International Drug Name Search

Optison


Generic Name: perflutren protein type a microsphere (Intravenous route)


per-FLOO-tren PROE-teen type A MYE-kroe-sfeers


Intravenous route(Suspension)

Serious cardiopulmonary reactions, including fatalities, have occurred during or following perflutren-containing microsphere administration. Monitor vital signs, electrocardiography, and cutaneous oxygen saturation during and for at least 30 minutes after perflutren-containing microsphere administration in patients with pulmonary hypertension or unstable cardiopulmonary conditions, and have resuscitation equipment and trained personnel available .



Commonly used brand name(s)

In the U.S.


  • Optison

Available Dosage Forms:


  • Suspension

Therapeutic Class: Diagnostic Agent, Cardiac Function


Uses For Optison


The albumin microspheres sonicated preparation is an ultrasound contrast agent. Ultrasound contrast agents are used to help provide a clear picture during ultrasound. Ultrasound is a special kind of diagnostic procedure. It uses high-frequency sound waves to create images or “pictures” of certain areas inside the body. The sound waves produced by the ultrasound equipment can be reflected (bounced off) by different parts of the body, like for example, the heart. As the sound waves return they are electronically converted into images on a television screen. Unlike x-rays, ultrasound does not involve ionizing radiation.


The albumin microspheres sonicated preparation contains very small gas-filled albumin microspheres that reflect the sound waves and help create a better picture. The albumin microspheres sonicated preparation is given by injection into a vein before ultrasound to help diagnose problems of the heart.


The albumin microspheres sonicated preparation is to be given only by or under the direct supervision of a doctor with specialized training in ultrasound procedures.


Before Using Optison


In deciding to use a diagnostic test, any risks of the test must be weighed against the good it will do. This is a decision you and your doctor will make. Also, other things may affect test results. For this test, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Studies on this agent have been done only in adult patients, and there is no specific information comparing use of albumin microspheres sonicated in children with use in other age groups.


Geriatric


Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults. There is no specific information comparing use of albumin microspheres sonicated in the elderly with use in other age groups.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this diagnostic test. Make sure you tell your doctor if you have any other medical problems, especially:


  • Congenital heart defects or

  • Heart shunt or

  • Liver problems—Use of the albumin microspheres sonicated preparation is not recommended because its effect when these conditions are present is not known

Proper Use of Optison


Your doctor may have special instructions for you in preparation for your test. If you do not understand the instructions you receive or if you have not received such instructions, check with your doctor in advance.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


Precautions While Using Optison


There are no special precautions to observe after having this test.


Optison Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


Less common or rare
  • Chest pain; difficulty breathing or shortness of breath; itching; skin rash

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Dizziness; flushing of skin or sensation of warmth; headache; nausea and/or vomiting

Less common
  • Changes in taste; dryness of mouth; fatigue; pain at injection site; weakness

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Optison side effects (in more detail)



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More Optison resources


  • Optison Side Effects (in more detail)
  • Optison Use in Pregnancy & Breastfeeding
  • Optison Drug Interactions
  • Optison Support Group
  • 0 Reviews · Be the first to review/rate this drug


  • Optison MedFacts Consumer Leaflet (Wolters Kluwer)

  • Optison Prescribing Information (FDA)

  • Perflutren Professional Patient Advice (Wolters Kluwer)

  • Definity MedFacts Consumer Leaflet (Wolters Kluwer)

  • Definity Prescribing Information (FDA)