VABRINTY (LEUPROLIDE ACETATE)
Summary
FDA approved VABRINTY (LEUPROLIDE ACETATE) by TOLMAR. NDA (New Drug) approval (Labeling) on 2026-05-06. POWDER, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
NDA021343-60
Action Date
2026-05-06
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
VABRINTY (generic: LEUPROLIDE ACETATE), POWDER, SUBCUTANEOUS. Application: NDA021343
Company
Context & Analysis
TOLMAR has 4 FDA actions in our database.
Frequently Asked Questions
How often does TOLMAR have FDA actions?
TOLMAR has 4 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA021343-60" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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