YEZTUGO (LENACAPAVIR SODIUM)
Summary
FDA approved YEZTUGO (LENACAPAVIR SODIUM) by GILEAD SCIENCES INC. NDA (New Drug) approval (Type 10 - New Indication Submitted as Distinct NDA - Not Consolidated) on 2025-06-18. SOLUTION, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
NDA220018-1
Action Date
2025-06-18
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
YEZTUGO (generic: LENACAPAVIR SODIUM), SOLUTION, SUBCUTANEOUS. Application: NDA220018
Company
Context & Analysis
GILEAD SCIENCES INC has 11 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
How often does GILEAD SCIENCES INC have FDA actions?
GILEAD SCIENCES INC has 11 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA220018-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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