VABOMERE (MEROPENEM-VABORBACTAM)
Summary
FDA approved VABOMERE (MEROPENEM-VABORBACTAM) by REMPEX. NDA (New Drug) approval (Labeling) on 2026-02-20. POWDER, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA209776-10
Action Date
2026-02-20
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
VABOMERE (generic: MEROPENEM-VABORBACTAM), POWDER, INTRAVENOUS. Application: NDA209776
Company
Context & Analysis
REMPEX has 2 FDA actions in our database.
Frequently Asked Questions
How often does REMPEX have FDA actions?
REMPEX has 2 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 "NDA209776-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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