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MabThera® Concentrate for Infusion for Clinics
$2,199.00
Description
MabThera is a rituximab monoclonal antibody concentrate for preparation and intravenous infusion in specialist settings. Oncology, hematology, and rheumatology services stock this reference product to support B‑cell–directed protocols and coordinated infusion schedules. Our US distribution helps credentialed facilities maintain predictable access.
What MabThera Is and How It Works
MabThera® contains rituximab, a chimeric monoclonal antibody that targets the CD20 antigen on B lymphocytes. By binding CD20, it facilitates B‑cell depletion, which can support protocols within hematologic oncology and immune-mediated disease programs. Administration is by intravenous infusion under trained supervision in accordance with institutional procedures. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
This preparation is positioned for use in professional infusion suites, inpatient units, and designated ambulatory centers. It integrates with standard pharmacy compounding steps before IV administration. Catalog notation may reference mabthera non english to indicate the packaging language of the supplied units. For related categories, see Pharmaceuticals.
Professional Applications
Clinics deploy this anti‑CD20 class agent within multidisciplinary infusion programs. Pharmacy teams prepare the concentrate for solution per facility protocols, while nursing staff monitor patients during and after infusion. It fits oncology day‑unit workflows, hematology cycles, and rheumatology pathways that schedule premedication, line access, observation, and documentation.
Service lines that manage immune conditions may also coordinate adjunct therapies and supportive agents across cycles. Workflow alignment with scheduling, chair time, staff assignments, and pharmacy cutoffs remains straightforward because the product follows established infusion standards. For service breadth across musculoskeletal care, review Rheumatology and injectables such as Orthovisc ENG.
Order MabThera IV infusion vials.
Key Features
- CD20-targeted mAb: rituximab for B‑cell–directed protocols.
- IV concentrate format: prepared for infusion under aseptic conditions.
- Professional administration: trained clinicians supervise infusion and monitoring.
- Quality and compliance: manufactured to recognized GMP standards.
- MabThera non-English packaging: language may differ from US packs; verify locally.
- Clear identification: lot number and expiry printed on pack and vial labels.
- Program fit: aligns with oncology, hematology, and rheumatology infusion setups.
- Risk controls: pre-infusion infection screening per facility policy.
Benefits in Practice
Infusion teams value consistent product identity and labeling that supports pharmacy checks, chain‑of‑custody, and bedside verification. The presentation integrates with existing aseptic preparation steps, IV administration sets, and observation protocols, minimizing workflow disruption. Standardized pack labeling helps streamline reconciliation across multi‑site networks and satellite pharmacies.
Purchasing leads can align contracting with expected cycles and clinic volumes, reducing ad‑hoc reorders. Documentation is simplified because attributes such as lot and expiry are readily visible for electronic capture. Your finance team can track MabThera infusion vial cost within established cost‑center reporting and preferred vendor agreements. For class context on infusion biologics, see the in‑depth Remicade Overview.
Composition & Ingredients
Active ingredient: rituximab, a chimeric monoclonal antibody directed against CD20 on B lymphocytes. The excipient system, stabilizers, and diluents follow the manufacturer’s specifications for the intended concentrate for solution. Refer to the outer carton, vial label, and enclosed leaflet for the full qualitative composition and any buffer components. Facilities should consult their formulary monograph and the manufacturer’s documentation to confirm compatibility, storage conditions, and handling requirements at the time of receipt.
Packaging & Supply
This listing is supplied with a MabThera Non-English label. Carton and vial labels include product name, lot number, and expiry date for inventory control. Packaging language may vary by origin; pharmacy should confirm equivalence to internal formulary entries and update electronic systems accordingly. Always align local barcode capture and shelf identifiers with your EHR and inventory modules.
SKU: 88866. Units are intended for hospital and clinic use, with labeling and directions provided by the manufacturer. Strength, preparation details, and storage instructions appear on the pack and leaflet; verify against your institutional protocol before first use in a new lot. For manufacturer lineage, see MabThera Roche.
Ordering & Logistics
Account verification is required prior to purchase. Once approved, sign in to view contract tiers and submit purchase orders. Your team can coordinate shipping windows with infusion schedules and pharmacy receiving hours. Order rituximab IV infusion vials within your standard procurement workflow.
We support temperature-controlled handling when required and tracked US delivery. Your facility can upload license documents during onboarding, assign approved buyers, and enable purchase controls. For scheduling consistency, align order cutoffs with compounding calendars, chair allocations, and prescriber rosters. Contact customer support if you need documentation for formulary review or vendor setup.
Comparable Products
Clinics evaluating anti‑inflammatory or immunology infusion options sometimes consider other biologics within their service lines. Review Remicade Non-English or Entyvio Non-English as category comparators for program planning and resource allocation.
Pricing & Access
Sign in to view institutional pricing based on verified licensure, order frequency, and volume commitments. Contracted tiers may be available for multi‑site organizations, outpatient infusion centers, and health systems. Group purchasing arrangements can be linked to your account to align formulary access and procurement controls. For transparent clinic procurement, unit‑level and carton‑level details are displayed in the portal alongside lot and expiry data once logged in.
Availability & Substitutions
Supply can vary by lot and market. If a requested presentation is unavailable, your pharmacy lead should review acceptable substitutes with the prescriber and P&T guidelines before any change to therapy. Biosimilar or alternative agents may require updated orders, premedication adjustments, and scheduling changes. Order rituximab IV infusion vials only after confirming the product listing aligns with your formulary entry and barcode records.
For perspective on category dynamics and adjacent service lines that may affect infusion chair capacity and staffing, see the Prolia Guide.
Authoritative Sources
- Roche: MabThera Global Product Information
- FDA: Rituximab Prescribing Information
- NIH MedlinePlus: Rituximab
Ready to proceed? Sign in to confirm eligibility, view details, and add this preparation to your next clinical order.
Frequently Asked Questions
What does Non-English packaging mean for clinical use?
Non-English packaging indicates the manufacturer’s original carton and vial labels use a language other than English. The product itself is the same reference rituximab line. Pharmacy should verify the item against the formulary record, ensure barcode recognition, and file the leaflet translation if needed. Lot and expiry appear on the labels. Follow institutional policies for language verification and documentation before first use of a new lot in your facility.
How is this product supplied for infusion pharmacy workflows?
It is supplied as a concentrate intended for dilution and intravenous infusion under trained supervision. Pharmacy teams prepare the unit according to institutional aseptic procedures and the manufacturer’s instructions on the carton and leaflet. Labels provide clear product identity, lot, and expiry for inventory control and documentation. Coordinate receiving with compounding schedules, chair time, and prescriber orders to support efficient infusion operations.
What verification is required before ordering?
A verified clinical account is required. Your facility will provide licensure documentation, authorized purchaser details, and shipping information during onboarding. After approval, sign in to view pricing and submit purchase orders. Many organizations also add purchase controls, such as PO requirements and approver workflows, to align procurement with internal policies and audit trails.
Can this product be used alongside other regimens?
Combination use is determined by the prescriber and your institution’s protocols. The product is often incorporated within multi‑agent care plans in oncology or immune‑mediated disease programs. Pharmacists should review compatibility, sequencing, and premedication requirements against current guidelines. Always follow local policies for regimen changes, monitoring, and documentation when integrating any biologic into established pathways.
What should clinics know about storage and handling?
Storage and handling requirements are stated on the manufacturer’s label and leaflet. Maintain required temperature ranges and protect from conditions that could compromise integrity. Use tamper‑evident inspection at receiving, and record lot and expiry. Before first use of a new lot, pharmacy should confirm storage parameters in the formulary system and educate nursing on any handling specifics cited on the label.
How do you handle lot and expiry documentation?
Every shipment displays lot number and expiry on the outer carton and vial. Your team can capture this data at receiving and again during compounding or administration, depending on policy. Electronic documentation is supported by aligning barcodes with the EHR and inventory module. Retain packing slips, certificates where applicable, and any translation aids for Non‑English labels in your quality files.
Is this item available to GPO or health system contract tiers?
Eligible organizations may access tiered pricing based on licensure, volumes, and agreements. Once your account is verified, you can request linkage to your GPO or health system contract, if applicable. Tier assignment considers order quantity, frequency, and service setting. Sign in to view available tiers and coordinate with your purchasing lead for alignment with your institution’s procurement framework.
Specifications
- Main Ingredient:
- Manufacturer: roche
- Drug Class:
- Generic Name: rituximab
- Package Contents: 50 mL (10 mg/mL) x 1 Vial
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
Mabthera/Roche
Here to help
Questions about ordering, delivery or products? You can email our team here or call now at 1-800-630-9757 and be connected with your dedicated Account Manager
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