Generic Binosto Availability

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

BINOSTO (alendronate sodium - tablet, effervescent; oral)

  • Manufacturer: MISSION PHARMA
    Approval date: March 12, 2012
    Strength(s): EQ 70MG BASE [RLD]

Has a generic version of Binosto been approved?

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

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

  • Effervescent compositions comprising bisphosphonates and methods related thereto
    Patent 7,488,496
    Issued: February 10, 2009
    Inventor(s): Rosen; Christer
    The invention provides effervescent composition comprising a bisphosphonate, an acidic compound, an alkaline effervescing component, and optionally an anti-ulcer agent and methods of treating osteoporosis in a mammal using the effervescent compositions.
    Patent expiration dates:
    • August 11, 2023
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      Drug substance
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      Drug product
  • Effervescent compositions comprising phosphonates and methods related thereto
    Patent 7,964,212
    Issued: June 21, 2011
    Inventor(s): Rosen; Christer
    The invention provides effervescent composition comprising a bisphosphonate, an acidic compound, an alkaline effervescing component, and optionally an anti-ulcer agent and methods of treating osteoporosis in a mammal using the effervescent compositions.
    Patent expiration dates:
    • March 6, 2023
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      Drug substance
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      Drug product

See also...

Glossary

TermDefinition
Drug PatentA 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 ExclusivityExclusivity 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.
RLDA 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.
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