NDC Code | 72426-818-03 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72426-818-03) |
Product NDC | 72426-818 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Nexlizet |
Non-Proprietary Name | Bempedoic Acid And Ezetimibe |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20200309 |
Marketing Category Name | NDA |
Application Number | NDA211617 |
Manufacturer | Esperion Therapeutics, Inc. |
Substance Name | BEMPEDOIC ACID; EZETIMIBE |
Strength | 180; 10 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adenosine Triphosphate-Citrate Lyase Inhibitor [EPC], Adenosine Triphosphate-Citrate Lyase Inhibitors [MoA], Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC] |