Solriamfetol Hydrochloride | ||||
CAS NO.: | 178429-65-7 | |||
Chemical Formula: | C10H15ClN2O2 | |||
Molecular Weight: | 230.6900 | |||
DMF&GMP status: | Please contact us for more details. | Description: |
Solriamfetol marketed under the brand name Sunosi by Jazz Pharmaceuticals in the United States is a dopamine and norepinephrine reuptake inhibitor (DNRI) indicated in treating daytime sleepiness associated with narcolepsy or obstructive sleep apnea. Solriamfetol was given FDA approval in 2019.
**The products protected by patents in this product catalog are used for laboratory analysis, research and development, and cannot be sold to any country or region with patent protection and for commercial purpose. If the resulting patent infringement risks and responsibilities will be borne by the buyer. |
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Approvals | ||||
Active Ingredient | Dosage Form; Route | Strength | Proprietary Name | Applicant |
SOLRIAMFETOL HYDROCHLORIDE | TABLET;ORAL | EQ 75MG BASE | SUNOSI | JAZZ PHARMACEUTICALS IRELAND LTD |
SOLRIAMFETOL HYDROCHLORIDE | TABLET;ORAL | EQ 150MG BASE | SUNOSI | JAZZ PHARMACEUTICALS IRELAND LTD |
Patent Data | ||||
Patent No. | Patent Expiration | Drug Substance Claim | Drug Product Claim | Patent Use Code |
8440715 | 08/25/2027 | U-2548 | ||
8877806 | 06/07/2026 | U-2548 | ||
9604917 | 06/07/2026 | U-2548 | ||
10195151 | 09/05/2037 | DP | ||
10351517 | 06/07/2026 | U-2548 | ||
10512609 | 09/05/2037 | U-2548 | ||
Exclusive Data | ||||
Exclusivity Code | Exclusivity Expiration | |||
NCE | 06/17/2024 | |||
ODE-254 | 06/17/2026 | |||