Generic Menostar Availability
Menostar is a brand name of estradiol, approved by the FDA in the following formulation(s):
MENOSTAR (estradiol - film, extended release; transdermal)
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Manufacturer: BAYER HLTHCARE
Approval date: June 8, 2004
Strength(s): 0.014MG/24HR [RLD]
Has a generic version of Menostar been approved?
No. There is currently no therapeutically equivalent version of Menostar available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Menostar. 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.
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Methods for treating postmenopausal women using ultra-low doses of estrogen
Patent 5,891,868
Issued: April 6, 1999
Inventor(s): Cummings; Steven & Ellman; Herman & Ettinger; Bruce
Assignee(s): Kaiser Foundation Health Plan, Inc. Permanente Medical Group, Inc. The Regents of the University of California Berlex Laboratories
The present invention provides methods for treating physical conditions resulting from postmenopausal estrogen decline in a postmenopausal subject, and in particular methods for reducing the risk of osteoporotic bone fractures in a postmenopausal subject. The present invention also provides a kit useful for carrying out the methods of the present invention.Patent expiration dates:- November 21, 2017✓✓
- November 21, 2017
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Methods for treating postmenopausal women using ultra-low doses of estrogen
Patent 6,692,763
Issued: February 17, 2004
Inventor(s): Steven R.; Cummings & Bruce; Ettinger & Herman; Ellman
Assignee(s): The Regents of the University of California Kaiser Foundation Health Plan, Inc. The Permanente Medical Group, Inc. Berlex Laboratories, Inc.
The present invention provides methods for treating physical conditions resulting from postmenopausel estrogen decline in a postmenopausel subject, and in particular methods for reducing the risk of osteoporotic bone fractures in a postmenopausal subject. The present invention also provides a kit for carrying out the methods of the present invention.Patent expiration dates:- November 21, 2017✓✓
- November 21, 2017
See also...
- Menostar Consumer Information (Drugs.com)
- Menostar weekly patch Consumer Information (Wolters Kluwer)
- Menostar Consumer Information (Cerner Multum)
- Menostar Transdermal Advanced Consumer Information (Micromedex)
- Estradiol Consumer Information (Drugs.com)
- Estring ring Consumer Information (Wolters Kluwer)
- Estradiol Consumer Information (Wolters Kluwer)
- Estradiol acetate Consumer Information (Wolters Kluwer)
- Estradiol cypionate Consumer Information (Wolters Kluwer)
- Estradiol gel Consumer Information (Wolters Kluwer)
- Estradiol patch Consumer Information (Wolters Kluwer)
- Estradiol ring Consumer Information (Wolters Kluwer)
- Estradiol spray Consumer Information (Wolters Kluwer)
- Estradiol valerate Consumer Information (Wolters Kluwer)
- Estradiol weekly patch Consumer Information (Wolters Kluwer)
- Estradiol injection Consumer Information (Cerner Multum)
- Estradiol oral Consumer Information (Cerner Multum)
- Estradiol topical for use on skin Consumer Information (Cerner Multum)
- Estradiol transdermal Consumer Information (Cerner Multum)
- Estradiol vaginal Consumer Information (Cerner Multum)
- Estradot Transdermal Therapeutic System Transdermal Advanced Consumer Information (Micromedex)
- Estradot Transdermal Transdermal Advanced Consumer Information (Micromedex)
- Estring Vaginal Advanced Consumer Information (Micromedex)
- Rhoxal-Estradiol Derm 50 Transdermal Advanced Consumer Information (Micromedex)
- Rhoxal-Estradiol Derm 75 Transdermal Advanced Consumer Information (Micromedex)
- Roxal-Estradiol Derm 100 Transdermal Advanced Consumer Information (Micromedex)
- Vagifem Vaginal Advanced Consumer Information (Micromedex)
- Vivelle 100 Mcg Transdermal Advanced Consumer Information (Micromedex)
- Vivelle 25 Mcg Transdermal Advanced Consumer Information (Micromedex)
- Vivelle 37.5 Mcg Advanced Consumer Information (Micromedex)
- Estradiol Transdermal Advanced Consumer Information (Micromedex)
- Estradiol Vaginal Advanced Consumer Information (Micromedex)
- Estradiol AHFS DI Monographs (ASHP)
Glossary
| Term | Definition |
|---|---|
| Drug Patent | A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation. |
| Drug Exclusivity | Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. |
| RLD | A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. |


