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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 211616
Company: ESPERION THERAPS INC

Products on NDA 211616

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NEXLETOL	BEMPEDOIC ACID	180MG	TABLET;ORAL	Prescription	None	Yes	Yes

Approval Date(s) and History, Letters, Labels, Reviews for NDA 211616

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
02/21/2020	ORIG-1	Approval	Type 1 - New Molecular Entity	STANDARD	Label (PDF) Letter (PDF) Review		https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/211616s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/211616Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2020/211616Orig1s000TOC.html

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
01/09/2026	SUPPL-26	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/211616s026lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2026/211616Orig1s026ltr.pdf
11/21/2025	SUPPL-24	Efficacy-New Indication	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s024lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/211616Orig1s024ltr.pdf
07/21/2025	SUPPL-23	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s022s023lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/211616Orig1s022, s023ltr.pdf
07/21/2025	SUPPL-22	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s022s023lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/211616Orig1s022, s023ltr.pdf
12/13/2023	SUPPL-15	Labeling-Package Insert, Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211616s015lbl.pdf
09/20/2023	SUPPL-14	Labeling-Package Insert	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211616s014lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/211616Orig1s014;211617Orig1s018ltr.pdf
03/22/2024	SUPPL-13	Efficacy-New Indication	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/211616s012s013lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/211616Orig1s012; s013ltr.pdf
03/22/2024	SUPPL-12	Efficacy-New Indication	Label (PDF) Letter (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/211616s012s013lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/211616Orig1s012; s013ltr.pdf

Labels for NDA 211616

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
01/09/2026	SUPPL-26	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/211616s026lbl.pdf
11/21/2025	SUPPL-24	Efficacy-New Indication	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s024lbl.pdf
07/21/2025	SUPPL-23	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s022s023lbl.pdf
07/21/2025	SUPPL-22	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/211616s022s023lbl.pdf
03/22/2024	SUPPL-13	Efficacy-New Indication	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/211616s012s013lbl.pdf
03/22/2024	SUPPL-12	Efficacy-New Indication	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/211616s012s013lbl.pdf
12/13/2023	SUPPL-15	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211616s015lbl.pdf
12/13/2023	SUPPL-15	Labeling-Patient Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211616s015lbl.pdf
09/20/2023	SUPPL-14	Labeling-Package Insert	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211616s014lbl.pdf
02/21/2020	ORIG-1	Approval	Label (PDF)		https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/211616s000lbl.pdf

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