Meropenem-vaborbactam
Limited reviewed summaryFull monograph review pending
No original GlobalRPh dilution article is available for this record.
Reviewed product information
Vabomere adult single-dose vial, meropenem 1 g and vaborbactam 1 g for IV infusion.
Use U.S. label section 2.3, Table 2 for bag volumes and final concentrations. The Galway examples assume a different bag preparation and final volume.
Preparation sources checked 2026-11-13.
Reconstitution
Reconstitute each vial with 20 mL of 0.9% sodium chloride injection. Gently dissolve the powder. The volume in the vial is approximately 21.3 mL.
Sources and exact locations
Claim ID: IVR-70-MEROPENEM-VABORBACTAM-001
Review basis: Separately authored institutional guidance
Source 1
VABOMERE U.S. prescribing information (opens in a new tab)
Exact location: Section 2.3, Preparation and Table 2 (SPL section 48b14b9d-edb4-4d85-baf0-06c6e604f26a)
Publisher: DailyMed / Melinta Therapeutics, LLC
Source family: U.S. product prescribing information
Retrieved: 2026-11-13T14:23:07.312855+00:00
Source 2
Galway adult IV guide: Meropenem-vaborbactam (opens in a new tab)
Exact location: Reconstitution
Publisher: Galway University Hospitals Medicines Information
Source family: Galway University Hospitals Medicines Information
Retrieved: 2026-11-13T14:23:07.512416+00:00
Separately edited hospital guidance may draw on product labeling. Only overlapping preparation steps are used.
Dilution
Use 0.9% sodium chloride injection for further dilution. Choose the bag size and vial withdrawal for the ordered dose from the U.S. preparation table.
Sources and exact locations
Claim ID: IVR-70-MEROPENEM-VABORBACTAM-002
Review basis: Separately authored institutional guidance
Source 1
VABOMERE U.S. prescribing information (opens in a new tab)
Exact location: Section 2.3, Preparation and Table 2 (SPL section 48b14b9d-edb4-4d85-baf0-06c6e604f26a); 2.4 Drug Compatibility (SPL section 14a9cb4b-df73-4f9d-b49b-1c531e424c77)
Publisher: DailyMed / Melinta Therapeutics, LLC
Source family: U.S. product prescribing information
Retrieved: 2026-11-13T14:23:07.312855+00:00
Source 2
Galway adult IV guide: Meropenem-vaborbactam (opens in a new tab)
Exact location: Infusion fluids and Methods of intravenous administration
Publisher: Galway University Hospitals Medicines Information
Source family: Galway University Hospitals Medicines Information
Retrieved: 2026-11-13T14:23:07.512416+00:00
Separately edited hospital guidance may draw on product labeling. Only overlapping preparation steps are used.
Infusion Time
Administer the diluted adult dose over 3 hours.
Sources and exact locations
Claim ID: IVR-70-MEROPENEM-VABORBACTAM-003
Review basis: Separately authored institutional guidance
Source 1
VABOMERE U.S. prescribing information (opens in a new tab)
Exact location: 2.1 Recommended Dosage (SPL section fb9778d3-3ee1-43ba-ae4d-39dff4d9c861)
Publisher: DailyMed / Melinta Therapeutics, LLC
Source family: U.S. product prescribing information
Retrieved: 2026-11-13T14:23:07.312855+00:00
Source 2
Galway adult IV guide: Meropenem-vaborbactam (opens in a new tab)
Exact location: Methods of intravenous administration
Publisher: Galway University Hospitals Medicines Information
Source family: Galway University Hospitals Medicines Information
Retrieved: 2026-11-13T14:23:07.512416+00:00
Separately edited hospital guidance may draw on product labeling. Only overlapping preparation steps are used.
Product identifiers and clinical review status
Selected prescribing information available. Full monograph review pending.
Selected product identity
Matched to U.S. product NDC 70842-120 for the preparation statements shown.
View product identifiers and primary-label provenance
- Selected product scope
- Vabomere adult single-dose vial, meropenem 1 g and vaborbactam 1 g for IV infusion.
- Labeler
- Melinta Therapeutics, LLC
- Application number(s)
- NDA209776
- NDC(s)
- 70842-120-01; 70842-120-06
- DailyMed Set ID
- e237fd0f-3050-42a3-b43e-b6fb4824e93d
- SPL version
- 14
- Label printed revision date
- Not established
- SPL effective date
- 2026-02-27
- Retrieved
- 2026-11-13T14:23:07.312855+00:00
- Downloaded XML SHA-256
- 1228d707b3423beb564102aada6fe233febf1dcba2f5bc845d5f27bf06131fd7
What remains to be completed
- Extract and verify presentation-specific IV preparation.
- Complete indication- and age-specific dosing, incompatibility, monitoring and stability review.
- Assess any proposed compounding BUD for the exact formulation, concentration, container and conditions.