Eligible patients may qualify for Camber’s copay assistance program, including eligible commercially insured patients and eligible cash-paying patients without primary insurance. Qualified patients may pay as little as $0 out of pocket.*
Sodium Oxybate Oral Solution is indicated for the treatment of cataplexy or excessive daytime sleepiness (EDS) in patients with narcolepsy.
Sodium Oxybate Oral Solution carries a boxed warning for central nervous system (CNS) depression and abuse and misuse. Taking Sodium Oxybate with other Central Nervous System (CNS) depressants has been associated with trouble breathing (respiratory depression), low blood pressure (hypotension), changes in alertness (drowsiness), fainting (syncope), and death. Sodium Oxybate is a form of gamma hydroxybutyrate (GHB). Abuse or misuse of illegal GHB alone or with other CNS depressants (drugs that cause changes in alertness or consciousness) may result in seizures, trouble breathing (respiratory depression), changes in alertness (drowsiness), coma, and death. Patients on Sodium Oxybate should be monitored for confusion, anxiety, and suicidality. Because of these risks, Camber Pharmaceuticals’ Sodium Oxybate is available only through the shared Sodium Oxybate REMS Program. Patients must be enrolled in the shared Sodium Oxybate REMS Program to receive Camber Pharmaceuticals’ Sodium Oxybate Oral Solution. For full prescribing information, see package insert.
Camber Pharmaceuticals’ Sodium Oxybate is a Schedule III controlled substance and is available only through the shared Sodium Oxybate REMS Program due to the risks of central nervous system (CNS) depression and abuse/misuse. Patients must be enrolled in the shared Sodium Oxybate REMS Program to receive Camber Pharmaceuticals’ Sodium Oxybate Oral Solution.
In the U.S., 9 out of 10 prescriptions filled are for generic drugs, which help lower healthcare costs and improve access by increasing market competition. The FDA’s Office of Generic Drugs rigorously reviews each proposed generic to ensure it matches the brand-name version in active ingredients, strength, dosage form, and route of administration. FDA-approved generics must perform the same in the body, meet the same high standards for quality, strength, purity, and stability, and are manufactured in facilities that meet the same strict requirements as brand-name drugs.
Learn more on the FDA’s website: https://www.fda.gov/drugs/buying-using-medicine-safely/generic-drugs
For any inquires related to adverse events and product complaints please contact us Toll Free at 1-866-495-1995 or email us at druginfo@camberpharma.com. Any information about prescription products and their uses, patients/consumers should call their doctor or pharmacist.