Generic Libervant Availability
Last updated on Jun 12, 2024.
Libervant is a brand name of diazepam, approved by the FDA in the following formulation(s):
LIBERVANT (diazepam - film;buccal)
-
Manufacturer: AQUESTIVE
Approval date: April 26, 2024
Strength(s): 5MG [RLD], 7.5MG [RLD], 10MG [RLD], 12.5MG [RLD], 15MG [RLD]
Has a generic version of Libervant been approved?
No. There is currently no therapeutically equivalent version of Libervant available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Libervant. 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.
-
Pharmaceutical compositions with enhanced permeation
Patent 11,273,131
Issued: March 15, 2022
Inventor(s): Schobel Alexander Mark & Varjan Stephanie Marie & Wargacki Stephen Paul
Assignee(s): AQUESTIVE THERAPEUTICS, INC.Pharmaceutical compositions having enhanced active component permeation properties are described.
Patent expiration dates:
- June 18, 2038✓
- June 18, 2038
Related exclusivities
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
Exclusivity expiration dates:
- April 26, 2027 - NEW PRODUCT
More about Libervant (diazepam)
- Check interactions
- Compare alternatives
- Pricing & coupons
- Latest FDA alerts (2)
- Side effects
- Dosage information
- During pregnancy
- FDA approval history
- Drug class: benzodiazepine anticonvulsants
- Breastfeeding
Patient resources
Other brands
Valium, Diastat AcuDial, Valtoco, Diastat, ... +3 more
Professional resources
Other brands
Related treatment guides
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.