Generic Baqsimi Availability
Last updated on Apr 10, 2025.
Baqsimi is a brand name of glucagon, approved by the FDA in the following formulation(s):
BAQSIMI (glucagon - powder;nasal)
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Manufacturer: AMPHASTAR PHARMS INC
Approval date: July 24, 2019
Strength(s): 3MG [RLD]
Is there a generic version of Baqsimi available?
No. There is currently no therapeutically equivalent version of Baqsimi available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Baqsimi. 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: Generic Drug FAQ.
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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Nasal powder formulation for treatment of hypoglycemia
Patent 10,213,487
Issued: February 26, 2019
Inventor(s): Mantripragada Sankaram & Piche Claude A. & Van Betsbrugge Jo Jan Filip
Assignee(s): Eli Lilly and CompanyThe present invention provides a powder formulation containing glucagon or a glucagon analog for nasal administration, useful in the treatment of hypoglycemia, and in particular the treatment of severe hypoglycemia. The present invention also provides a method of making this powder formulation, and to devices and methods for using the powder formulation.
Patent expiration dates:
- February 16, 2036✓✓
- February 16, 2036
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Medication delivery systems and methods
Patent 10,765,602
Issued: September 8, 2020
Inventor(s): Arnett Jaime Ray & Snow Andrew Thomas
Assignee(s): Eli Lilly and CompanyThe present disclosure relates to a medication delivery system including a medication administration device, a medication within the medication administration device, a container defining a cavity receiving the medication administration device, and a cap attached to the container and sealing the medication administration device within the cavity. The medication administration device includes an actuator extending from a body and operable to expel the medication by depressing the actuator into the body. The cap includes hold down members positioned to bear against the body of the medication administration device to prevent movement of the medication administration device toward the cap beyond a predetermined distance. The medication administration device is thereby prevented, inter alia, from prematurely discharging the medication during storage and transport.
Patent expiration dates:
- September 23, 2039✓
- September 23, 2039
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Device for dispensing a fluid product
Patent 10,894,133
Issued: January 19, 2021
Inventor(s): Baillet Matthieu & Carballo Dolorès & Dulude Hélène & Poullain Franck
Assignee(s): APTAR FRANCE SASA dispenser device for dispensing a fluid or powder composition, the dispenser device comprising: a dispenser head () that is provided with a dispenser outlet () that is formed at the end of a hollow sleeve (); an air expeller () for generating a flow of air while the device is being actuated, said air expeller including a piston () that slides in an air chamber () between a rest position and a dispensing position, said air chamber () including a cylindrical body in which said piston () slides in airtight manner; and a reservoir () that contains a single dose of composition, said reservoir () including an air inlet () that is connected to said air expeller (), and a composition outlet () that is connected to said dispenser outlet (), said air inlet () including a composition retainer member () for retaining the composition in the reservoir () until the composition is dispensed, and said composition outlet () being closed by a closure element () that is force fitted in the composition outlet () of the reservoir (); said device further comprising a mechanical opening system () that co-operates with said closure element () so as to expel it mechanically from its closed position while the device is being actuated; said device further comprising an indicator () that, in the rest position before actuation, is in a first state, and that after actuation passes into a second state, the passage from the first to the second state informing the user that the device has been actuated, said first state being a visible state and said second state being a non-visible state, said device including a pusher element () that is secured to said piston (), and on which the user presses during actuation, said dispenser head () including a skirt () that is arranged around said air chamber (), said pusher element (), in its rest position before actuation, projecting axially out from said skirt (), and after actuation, being arranged inside said skirt (), said pusher element () including an indicator () that is visible before actuation and that is not visible after actuation.
Patent expiration dates:
- January 3, 2038✓
- January 3, 2038
More about Baqsimi (glucagon)
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- Drug class: glucose elevating agents
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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. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
