Generic femhrt Availability
femhrt is a brand name of ethinyl estradiol/norethindrone, approved by the FDA in the following formulation(s):
FEMHRT (ethinyl estradiol; norethindrone acetate - tablet; oral)
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Manufacturer: WARNER CHILCOTT LLC
Approval date: January 14, 2005
Strength(s): 0.0025MG;0.5MG
Has a generic version of femhrt been approved?
No. There is currently no therapeutically equivalent version of femhrt available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of femhrt. 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 femhrt.
See also...
- Femhrt Consumer Information (Drugs.com)
- Femhrt Consumer Information (Wolters Kluwer)
- Femhrt 1 mg/5 mcg HRT Consumer Information (Cerner Multum)
- Femhrt 1/5 HRT Consumer Information (Cerner Multum)
- Femhrt HRT Consumer Information (Cerner Multum)
- Loestrin Fe Consumer Information (Wolters Kluwer)
- Microgestin Fe Consumer Information (Wolters Kluwer)
- Norethindrone/ethinyl estradiol Consumer Information (Wolters Kluwer)
- Norethindrone/ethinyl estradiol (HRT) Consumer Information (Wolters Kluwer)
- Norethindrone/ethinyl estradiol chewable tablets Consumer Information (Wolters Kluwer)
- Norethindrone/ethinyl estradiol tablets Consumer Information (Wolters Kluwer)
- Ethinyl estradiol and norethindrone Consumer Information (Cerner Multum)
- Ethinyl estradiol and norethindrone HRT Consumer Information (Cerner Multum)
- Norethindrone, ethinyl estradiol, and ferrous fumarate Advanced Consumer Information (Micromedex)
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. |


