SUNOSI is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Jazz Pharmaceuticals, Inc.. The primary component is Solriamfetol.
Product ID | 68727-351_34e0a7d5-0967-4fcb-9f90-0c2c7facc3ca |
NDC | 68727-351 |
Product Type | Human Prescription Drug |
Proprietary Name | SUNOSI |
Generic Name | Solriamfetol |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2019-06-18 |
Marketing Category | NDA / NDA |
Application Number | NDA211230 |
Labeler Name | Jazz Pharmaceuticals, Inc. |
Substance Name | SOLRIAMFETOL |
Active Ingredient Strength | 150 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-06-18 |
Marketing End Date | 2025-10-31 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA211230 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-18 |
Marketing Category | NDA |
Application Number | NDA211230 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-06-18 |
Marketing Category | NDA |
Application Number | NDA211230 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-18 |
Marketing Category | NDA |
Application Number | NDA211230 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-18 |
Ingredient | Strength |
---|---|
SOLRIAMFETOL | 150 mg/1 |
SPL SET ID: | 2f30ab12-20e1-4391-9359-24b23a21578d |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
68727-350 | SUNOSI | solriamfetol |
68727-351 | SUNOSI | solriamfetol |
81968-350 | SUNOSI | solriamfetol |
81968-351 | SUNOSI | solriamfetol |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUNOSI 87151190 5857817 Live/Registered |
Jazz Pharmaceuticals, Inc. 2016-08-25 |