Zurampic is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Ironwood Pharmaceuticals, Inc.. The primary component is Lesinurad.
Product ID | 70785-011_e0be03b1-e321-4297-b525-8151c03ab903 |
NDC | 70785-011 |
Product Type | Human Prescription Drug |
Proprietary Name | Zurampic |
Generic Name | Lesinurad |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2017-10-03 |
Marketing End Date | 2020-07-31 |
Marketing Category | NDA / NDA |
Application Number | NDA207988 |
Labeler Name | Ironwood Pharmaceuticals, Inc. |
Substance Name | LESINURAD |
Active Ingredient Strength | 200 mg/1 |
Pharm Classes | Urate Transporter 1 Inhibitor [EPC],Urate Transporter 1 Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA] |
NDC Exclude Flag | N |
Marketing Start Date | 2017-10-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA207988 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-03 |
Marketing End Date | 2020-07-31 |
Marketing Category | NDA |
Application Number | NDA207988 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-10-03 |
Marketing End Date | 2020-07-31 |
Ingredient | Strength |
---|---|
LESINURAD | 200 mg/1 |
SPL SET ID: | ef9e7711-f478-4e35-bf4e-6021c8457e3b |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0310-1475 | ZURAMPIC | lesinurad |
70785-011 | Zurampic | lesinurad |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ZURAMPIC 86488044 4865620 Live/Registered |
AstraZeneca AB 2014-12-22 |
![]() ZURAMPIC 86338542 4849004 Live/Registered |
AstraZeneca AB 2014-07-16 |