How to order VABOMERE® for your institution

Order VABOMERE® (meropenem and vaborbactam) using standard ordering procedure through your wholesaler

  • VABOMERE is a wholesaler-stocked product
  • If VABOMERE is not available at your wholesaler, the wholesaler can coordinate a drop shipment via Next Day Saver from a Melinta primary distribution provider
  • Download the Order Sheet for more information

VABOMERE comes in a box of 6 vials, the typical course of daily treatment*

How it’s supplied1:

VABOMERE is supplied as a white to light yellow sterile powder for constitution in single-dose, clear glass vials that contain 2 grams of VABOMERE. Each vial contains 1 gram of meropenem (equivalent to 1.14 grams of meropenem trihydrate), 1 gram of vaborbactam, and 0.575 gram of sodium carbonate.

ONE BOX is ONE DAY of treatment.*

VABOMERE 4 g (2 g meropenem and 2 g vaborbactam)



Each vial contains VABOMERE 2 g (1 g meropenem and 1 g vaborbactam) for injection and is supplied in a box of 6 vials.

Typical full course of daily treatment for patients with eGFR ≥50 mL/min/1.73 m2. Additional dosing information for patients with renal impairment can be found in the Dosing section of this website.

VABOMERE wholesaler contact information

VABOMERE is a wholesaler-stocked product. Please use standard ordering procedure through your wholesaler. If product is not available at your wholesaler, your wholesaler can easily coordinate a drop shipment via Next Day Saver from a Melinta primary distribution provider by calling your wholesaler‘s customer service number listed below.

Coding and reimbursement information for VABOMERE

Covers the coding requirements, coding systems, and their application when VABOMERE is administered

  • Lists ICD-10 codes and transition of care codes to facilitate timely claims processing and reduce the risk of denied claims
    –Includes the permanent J Code (J2186) for VABOMERE
  • Addresses coverage and payment information pertaining to Medicare, Medicaid, and commercial payers, in inpatient and outpatient settings, including long-term acute care and home infusion reimbursement
  • Includes sample CMS 1450 and CMS 1500 billing forms
  • See Coding and Billing Reference Guide for detail

Effective October 1, 2019: CMS has increased VABOMERE New Technology Add-On Payment (NTAP) coverage up to 75% for FY20202*

The Centers for Medicare & Medicaid Services (CMS) has approved VABOMERE for NTAP status. Medicare will now provide an add-on payment for VABOMERE of up to $8,316 per qualifying case to Inpatient Prospective Payment System (IPPS)-participating acute care hospitals. This add-on payment will be incremental to the MS-DRG reimbursement for qualifying Medicare inpatient cases.

*NTAP maximum payment for FY2019 (ending September 30, 2019) is 50% or up to $5,544 per admission.

About NTAP3,4

  • Helps ensure adequate payment for new medical services and technologies used to treat Medicare beneficiaries in the IPPS hospital setting
  • Provides an incremental reimbursement amount, in addition to the applicable MS-DRG–based reimbursement, for Medicare inpatient cases paid under the IPPS that involve the use of an eligible new medical service or technology
  • Offers a temporary stop-gap measure until MS-DRG can be recalibrated

VABOMERE is the only β-lactam-β-lactamase inhibitor with NTAP status2

Payment and Timing

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Under the IPPS system, costs are retrospectively reviewed on an annual basis in order to set the prospective DRG payment rates. Depending on the time of the introduction of the new technology, it can take 2 to 3 years before its cost is recognized in the recalibration of MS-DRG payment rates.3

Coding Information

In place of an ICD-10-PCS procedure code, cases of VABOMERE eligible for FY2020 NTAP will be paid with the following 11-digit NDC code in data element LIN03 of the 837i Health Care Claim Institutional form: 65293000901 or 70842012001.

The 11-digit NDC is required, and dashes are not allowed on the claim when inserting the code.


The content of the guides made available on this website are general in nature, strictly for informational purposes only, and do not cover all situations or all payers’ policies and guidance. The information provided in these guides were obtained from third-party sources and are subject to change without notice as a result of changes in reimbursement laws, regulations, rules, policies, and payment amounts. These guides are not intended to provide clinical practice guidelines.

Melinta Therapeutics, Inc. (Melinta) cannot guarantee, and is not responsible for, the payment of any claim. The coding, coverage, and payment of VABOMERE may vary by payer, plan, patient, and setting of care. Coding determinations and analysis should always be independently researched and assessed. For more information, please check with individual payers for specific coding, coverage, and payment requirements. It is the sole responsibility of the healthcare provider to code properly and to ensure the accuracy of all claims submitted for reimbursement. Additionally, as a prerequisite for submitting a claim, the provider is responsible for ensuring that all services are medically necessary and properly supported in the patient’s medical records.

Melinta specifically disclaims liability or responsibility for the results or consequences of any actions taken in reliance on information in provided in these guides.

References: 1. VABOMERE [package insert]: Melinta Therapeutics, Inc. 2. Centers for Medicare & Medicaid Services. Medicare Program: Hospital inpatient prospective payment systems for acute care hospitals and the long term care hospital prospective payment system and policy changes and fiscal year 2020 rates; quality reporting requirements for specific providers; Medicare and Medicaid promoting interoperability programs requirements for eligible hospitals and critical access hospitals [unpublished]. Fed Regist. Accessed August 8, 2019. 3. Additional payment for new medical services and technologies: general provisions, 42 CFR § 412.87 (2010). Published October 10, 2010. Accessed May 22, 2019. 4. Centers for Medicare & Medicaid Services. New medical services and new technologies. Published December 3, 2018. Accessed May 22, 2019.


VABOMERE® (meropenem and vaborbactam) is indicated for the treatment of patients 18 years of age and older with complicated urinary tract infections (cUTI) including pyelonephritis caused by the following susceptible microorganisms: Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae species complex.

To reduce the development of drug-resistant bacteria and maintain the effectiveness of VABOMERE and other antibacterial drugs, VABOMERE should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.



VABOMERE is contraindicated in patients with known hypersensitivity to any components of VABOMERE (meropenem and vaborbactam), or to other drugs in the same class or in patients who have demonstrated anaphylactic reactions to beta-lactam antibacterial drugs.

Warnings and Precautions

  • Hypersensitivity reactions were reported in patients treated with VABOMERE in the clinical trials. Serious and occasionally fatal hypersensitivity (anaphylactic) reactions and serious skin reactions have been reported in patients receiving therapy with beta-lactam antibacterial drugs. There have been reports of individuals with a history of penicillin hypersensitivity who have experienced severe hypersensitivity reactions when treated with another beta-lactam antibacterial drug. If an allergic reaction to VABOMERE occurs, discontinue the drug immediately.
  • Seizures and other adverse Central Nervous System (CNS) experiences have been reported during treatment with meropenem, which is a component of VABOMERE. Close adherence to the recommended dosage regimens is urged, especially in patients with known factors that predispose to convulsive activity.
  • Clostridium difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including VABOMERE, and may range in severity from mild diarrhea to fatal colitis. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents. If CDAD is suspected or confirmed, ongoing antibacterial drug use not directed against C. difficile may need to be discontinued.
  • The concomitant use of VABOMERE and valproic acid or divalproex sodium is generally not recommended. Case reports in the literature have shown that co-administration of carbapenems, including meropenem, to patients receiving valproic acid or divalproex sodium results in a reduction in valproic acid concentrations. The valproic acid concentrations may drop below the therapeutic range as a result of this interaction, therefore increasing the risk of breakthrough seizures. If administration of VABOMERE is necessary, consider supplemental anticonvulsant therapy.
  • In patients with renal impairment, thrombocytopenia has been observed in patients treated with meropenem, but no clinical bleeding has been reported.
  • Alert patients receiving VABOMERE on an outpatient basis regarding adverse reactions such as seizures, delirium, headaches and/or paresthesias that could interfere with mental alertness and/or cause motor impairment.
  • Prescribing VABOMERE in the absence of a proven or strongly suspected bacterial infection is unlikely to provide benefit to the patient and increases the risk of drug-resistant bacteria.
  • As with other antibacterial drugs, prolonged use of VABOMERE may result in overgrowth of nonsusceptible organisms.

Adverse Reactions

The most frequently reported adverse reactions occurring in ≥3% of patients treated with VABOMERE were headache, phlebitis/infusion site reactions, and diarrhea.

Please see full Prescribing Information.