Nexlizet is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Esperion Therapeutics, Inc.. The primary component is Bempedoic Acid; Ezetimibe.
Product ID | 72426-818_5dd83231-830c-482c-a341-d88c77c50c74 |
NDC | 72426-818 |
Product Type | Human Prescription Drug |
Proprietary Name | Nexlizet |
Generic Name | Bempedoic Acid And Ezetimibe |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2020-03-09 |
Marketing Category | NDA / NDA |
Application Number | NDA211617 |
Labeler Name | Esperion Therapeutics, Inc. |
Substance Name | BEMPEDOIC ACID; EZETIMIBE |
Active Ingredient Strength | 180 mg/1; mg/1 |
Pharm Classes | Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2020-03-09 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA211617 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-03-09 |
Marketing Category | NDA |
Application Number | NDA211617 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-03-09 |
Marketing Category | NDA |
Application Number | NDA211617 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-03-09 |
Ingredient | Strength |
---|---|
BEMPEDOIC ACID | 180 mg/1 |
SPL SET ID: | 3fa2108c-0300-47b8-9d34-f762af7c93c6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEXLIZET 88145092 not registered Live/Pending |
Esperion Therapeutics, Inc. 2018-10-05 |