Generic Seizalam Availability
Last updated on Jun 11, 2025.
Seizalam is a brand name of midazolam, approved by the FDA in the following formulation(s):
SEIZALAM (midazolam hydrochloride - solution;intramuscular)
-
Manufacturer: MMT
Approval date: September 14, 2018
Strength(s): EQ 50MG BASE/10ML (EQ 5MG BASE/ML) [RLD]
Is there a generic version of Seizalam available?
No. There is currently no therapeutically equivalent version of Seizalam available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Seizalam. 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 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:
- September 14, 2025 - TREATMENT OF STATUS EPILEPTICUS IN ADULTS
More about Seizalam (midazolam)
- Check interactions
- Compare alternatives
- Latest FDA alerts (4)
- Side effects
- Dosage information
- During pregnancy
- Drug class: benzodiazepines
- Breastfeeding
Patient resources
Other brands
Professional resources
Other brands
Related treatment guides
Related/similar drugs
Ativan
Ativan is a benzodiazepine used to treat anxiety disorders or anxiety associated with depression ...
Valium
Valium is used to treat anxiety disorders, alcohol withdrawal symptoms, or muscle spasms. Learn ...
Botox
Botox is used cosmetically to reduce facial lines and wrinkles and for medical purposes for ...
Dilantin
Dilantin (phenytoin) is an anti-epileptic drug used to control seizures. Includes Dilantin side ...
Versed
Versed is used for ICU Agitation, light anesthesia, light sedation
Nayzilam
Nayzilam (midazolam) is used to treat seizure clusters. Information includes Nayzilam side effects ...
Valtoco
Valtoco nasal spray is used for the acute treatment of intermittent seizure clusters (also known as ...
Pentobarbital
Pentobarbital is used for insomnia, sedation, status epilepticus
Phenytoin
Phenytoin is an anti-epileptic drug, also called an anticonvulsant. Learn about side effects ...
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.