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Description
What Xolair Is and How It Works
Xolair® is a subcutaneous monoclonal antibody used in professional settings for patients whose allergic asthma or chronic spontaneous urticaria remains uncontrolled on standard care. Clinics stock this biologic to support allergists, pulmonologists, and dermatologists who manage recurrent injection schedules and require consistent supply. We support US distribution to qualified facilities. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
This therapy targets circulating immunoglobulin E, which can help reduce downstream allergic inflammation signals. It is administered by subcutaneous injection at clinic visits, with the prescribing clinician determining the interval and total duration of therapy. Selection typically follows evaluation of clinical history and IgE levels, aligning the product with established specialty protocols.
Administration should occur under qualified medical supervision with post-injection observation according to clinic policy. This item is for prescription use only, not for at-home administration. For broader inventory planning, see our Pharmaceuticals category for additional agents used in specialty clinics.
Professional Applications
Clinics integrate this product into allergy and immunology programs where an injectable anti-IgE option supports ongoing disease management. Typical workflows include pre-visit assessment, medication preparation, subcutaneous administration, and observation periods. Teams document treatment rationale, timing, and any post-injection notes in the EHR to standardize care.
Programs may align visits on a 2 to 4 week cadence to match physician availability and patient scheduling preferences, with flexibility for add-on or catch-up sessions as clinically appropriate. Staff coordinate treatment rooms, medication checks, and ready access to emergency supplies during monitored administration.
For background reading on clinical roles and safety context, review our article Xolair Overview. Teams may additionally reinforce in-service training that emphasizes identification of hypersensitivity and appropriate response steps, supported by practical guidance such as Safety Protocols for injection-based workflows.
Key Features
- Anti-IgE mechanism: supports targeted allergy pathway management.
- Subcutaneous route: suited to office-based injection rooms.
- Clinic-administered only: professional preparation and oversight.
- Prescription product: qualified provider authorization required.
- Manufactured to high quality standards for sterile use.
- Single-use presentations: align with dose-specific preparation.
- Label clarity: lot and expiry visible to streamline tracking.
- Works with routine visit cycles for predictable scheduling.
Benefits in Practice
This product fits routine specialty visits, allowing teams to block injection slots alongside pulmonary, allergy, or dermatology consults. Staff can standardize preparation and observation steps, reducing variability between appointments and improving throughput in busy clinics. Consistent presentation also aids in pharmacy checks and nursing handoffs.
Inventory teams appreciate predictable reorder triggers and simple lot control, which supports audit readiness and recall response if needed. The line integrates with barcode workflows where used, assisting accurate charge capture and documentation. For procurement planning, many clinics track Omalizumab cost trends alongside payer policy updates and therapy pathway decisions.
Supply chain leads can coordinate forecasting based on scheduled appointments and expected additions from referral sources. See Clinic Procurement for considerations that may inform injection-room readiness and ancillary accessory selection.
Composition & Ingredients
The active component is omalizumab, a recombinant monoclonal antibody directed against IgE. As an Omalizumab injection, the formulation is designed for subcutaneous administration under professional supervision. Excipients may vary by presentation and should be reviewed on the package insert and product label prior to preparation.
Clinicians should consult the manufacturer’s prescribing information for complete details on composition, contraindications, warnings, and handling. Pharmacy and nursing teams must follow internal policies for biologic preparation and verification steps prior to patient administration.
Packaging & Supply
This biologic is supplied for single-patient use in clinic settings. Presentations are intended for subcutaneous injection after inspection and appropriate preparation steps. Labels display product name, lot number, and expiry to support inventory controls and documentation. Store and handle per the manufacturer’s label and your facility’s SOPs.
A Xolair® prescription from a qualified provider is required. Administration must occur in a clinical environment with appropriately trained staff and access to observation space and emergency response equipment. Please review the included professional materials before use.
Ordering & Logistics
Access is reserved for licensed healthcare facilities and prescribers with verified accounts. After approval, your team can place orders online, manage standing orders, and coordinate delivery windows that match clinic schedules. Account managers can assist with documentation requests, product education materials, or reordering support.
Verified purchasers may Buy omalizumab through the portal once credentials are confirmed. Shipments are directed to licensed practice addresses only. If your clinic requires synchronized arrivals for multiple locations, our team can help with staggered dispatch timing subject to availability and carrier constraints.
Comparable Products
Clinics evaluating immunology-focused biologics sometimes review alternatives in adjacent classes to support formulary decisions. Two commonly referenced options in our catalog include Saphnelo Injection and T-Cell Modulator. Selection should reflect prescriber judgment, labeled indications, safety profiles, and your facility’s therapeutic pathways.
Pricing & Access
Sign in to view contract tiers, request quotes, and confirm live availability. Volume-based arrangements and multi-site allocations may be available to qualified accounts. This section supports budget planning and formulary alignment across service lines where biologic injections are administered under supervision.
Facilities can Buy Xolair® through the portal once verification is complete. We also offer guidance on Xolair pricing strategies for clinics seeking consistent spend forecasts and a price for omalizumab that aligns with scheduled injection programs. Contact your account manager to discuss tiered structures, shipment cadence, and integration with your purchasing systems.
Availability & Substitutions
Supply may vary by presentation and timing. If a specific presentation is limited, your account manager can review alternatives that match your clinical workflow and storage capabilities. Always verify with the prescriber before any substitution to ensure alignment with the treatment plan and patient safety considerations.
Where therapeutic class alternatives are considered for institutional planning, teams sometimes evaluate options such as Integrin Therapy. Confirm indication, route, and operational fit before changes to clinic protocols.
Authoritative Sources
Ready to streamline your biologic supply program? Sign in to request inventory with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
Who can order this biologic from your platform?
Ordering is limited to licensed clinics, hospitals, and healthcare providers with verified accounts. We confirm practice credentials, shipping addresses, and any required state or institutional documentation before activating access. Once approved, you can place orders online, coordinate delivery windows, and work with an account manager for reorders. Residential or at‑home destinations are not eligible. This policy helps ensure professional oversight and regulatory compliance for clinic-administered injections.
How is this product typically handled in clinic settings?
Staff retrieve the unit from secure storage, confirm lot and expiry, and follow facility SOPs for inspection and preparation. A qualified provider authorizes administration and ensures observation after injection. Teams document medication details and post‑injection notes in the EHR. Clinics should maintain emergency equipment and trained personnel on site. Always consult the manufacturer’s label and your internal protocols for storage and handling requirements.
What visit cadence works best for operational planning?
Many programs organize recurring injections on two‑ to four‑week cycles, aligning with provider and patient scheduling. This cadence helps forecast staffing needs, room availability, and inventory pull times. Your prescriber determines the interval and therapy duration. Build in flexibility for rebooked or missed appointments. Pharmacy and nursing teams should coordinate to ensure product availability and observation capacity at each session.
Can this therapy be administered outside a monitored setting?
No. Administration should occur under qualified medical supervision with observation per your clinic policy. Teams should be prepared to recognize and respond to hypersensitivity or injection‑site reactions. This product is prescription‑only and not intended for at‑home use. Maintain readiness with appropriate emergency supplies on hand and follow local requirements and manufacturer guidance. Ensure all administration is documented in your EHR.
What documentation accompanies shipments for inventory control?
Shipments include a packing list and product labeling with lot and expiry details for your records. Many clinics scan or log these identifiers into their inventory systems to support traceability and recall readiness. If your site needs additional documentation for audits or purchasing systems, your account manager can help provide invoices or confirmations. Follow your facility’s chain‑of‑custody procedure when receiving and storing biologics.
How should teams prepare for first use at a new site?
Before first administration, verify storage conditions, create a standardized SOP, and train staff on inspection, preparation, and observation steps. Confirm that prescribers authorize in‑clinic use and that emergency equipment is available. Test EHR order sets, barcoding, and charge capture. Schedule initial patients with time for education and post‑injection monitoring. Coordinate with purchasing to ensure sufficient supply for planned visits and a buffer for reschedules.
Does this product integrate with common EHR and inventory systems?
Yes. Most clinics document administrations using standardized order sets and medication codes within their EHR, and track lots and expiries in inventory software or pharmacy modules. Barcoding can simplify verification and charge capture if your system supports it. Your team should validate that NDC mapping, scanning, and reporting workflows are configured correctly before go‑live to avoid reconciliation delays or stock discrepancies.
Specifications
- Main Ingredient:
- Manufacturer: Genentech, Inc.
- Drug Class:
- Generic Name: omalizumab
- Package Contents: 1 Injection
- Storage Requirements: Cool Temperature (2℃~8℃)
- Main Usage:
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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