Updated: January 19, 2026
Rabies Immune Globulin Shortage: What Providers and Prescribers Need to Know in 2026
Author
Peter Daggett

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No HRIG shortage exists nationally in 2026, but access issues remain real for rural patients. A clinical guide for providers on current availability, dosing nuances, and patient support resources.
For clinicians managing rabies post-exposure prophylaxis (PEP), the logistical challenges surrounding human rabies immune globulin (HRIG) can be significant — even when no formal shortage exists. This guide covers the current availability landscape, brand-specific considerations, dosing reminders, and how to support patients who face access or cost barriers.
Current Availability Status (2026)
The CDC confirms that as of 2026, there is no national shortage of human rabies immune globulin in the United States. Three FDA-licensed HRIG products are actively distributed:
HyperRAB (Grifols, 300 IU/mL): Available in 1 mL/300 IU and 5 mL/1,500 IU vials. Uses caprylate chromatography manufacturing process. Higher concentration requires careful attention to dosing — approximately half the volume needed compared to 150 IU/mL products.
KedRAB / KEDRAB (Kedrion/Kamada, 150 IU/mL): FDA-approved August 2017. Pediatric use label expansion in June 2021. Solvent/detergent treated.
Imogam Rabies-HT (Sanofi, 150 IU/mL): Heat-treated formulation available in the US since 1974. Established safety and efficacy record.
Critical Dosing Reminder: The HyperRAB Concentration Difference
A clinically significant point: HyperRAB is formulated at 300 IU/mL, while KedRAB and Imogam Rabies-HT are 150 IU/mL. The recommended dose for all products is 20 IU/kg body weight — but the volume required differs by twofold between these products.
Example: For a 70 kg patient, the required dose is 1,400 IU.
Using HyperRAB (300 IU/mL): 4.67 mL needed
Using KedRAB or Imogam (150 IU/mL): 9.33 mL needed
Note that when dilution is necessary to ensure sufficient volume to infiltrate all wound sites, HyperRAB should be diluted with D5W (dextrose 5% in water), not normal saline. Standard 150 IU/mL products can be diluted with normal saline. The CDC emphasizes care in ensuring the correct dose is administered to allow an adequate immune response.
ACIP PEP Protocol Review: Key Points for 2026
For previously unvaccinated patients, ACIP recommends:
Thorough wound cleansing with soap and water or povidone-iodine solution.
HRIG at 20 IU/kg on Day 0 — infiltrate as much as anatomically feasible into and around the wound; deliver any remaining volume IM at a site distant from the vaccine.
Rabies vaccine IM (deltoid) on Days 0, 3, 7, and 14.
For immunocompromised patients: add a 5th vaccine dose on Day 28 and check RVNA titer 7-14 days after the final dose.
Important reminders:
Never administer HRIG in the same syringe or same anatomical site as the first vaccine dose.
HRIG can be administered up to and including Day 7 if not available on Day 0 — but do not delay starting the vaccine.
Do not exceed the recommended dose of HRIG — higher doses can suppress the vaccine-induced active immune response.
Previously vaccinated patients (full series + confirmed titer) do NOT receive HRIG — only 2 vaccine doses (Day 0 and Day 3).
Access Challenges Your Patients May Face
Even without a formal shortage, patients encounter real-world access barriers:
Geographic access: Smaller rural facilities and urgent care centers often do not stock HRIG. Patients may need to travel to a larger hospital ER.
Cost barriers: The full PEP course can cost $2,500–$7,000 out of pocket. Some patients have delayed or avoided treatment due to cost — a potentially fatal decision. Manufacturer patient assistance programs exist through Sanofi, Grifols, and Kedrion.
Insurance prior authorization: Some payers require prior auth for PEP in outpatient settings. Most plans cover PEP when medically necessary after documented exposure — help patients navigate this proactively.
Helping Your Patients Find HRIG Quickly
For providers managing patients who need to locate a stocking facility — particularly those who received the first vaccine dose elsewhere or are following up — medfinder for providers is a service that contacts facilities near your patient to identify which ones carry HRIG, reducing the time spent on hold with facility pharmacy lines and helping ensure patients receive timely PEP.
Manufacturer Contact Information for HRIG
Grifols (HyperRAB): 1-800-520-2807
Kedrion/Kamada (KedRAB): 1-855-353-7466
Sanofi (Imogam Rabies-HT): 1-800-822-2463
Also see our companion provider guide: How to Help Your Patients Find Rabies Immune Globulin in Stock
Frequently Asked Questions
No. The CDC confirms there is no national shortage of human rabies immune globulin in the United States as of 2026. All three licensed brands (HyperRAB, KedRAB, Imogam Rabies-HT) are actively distributed. Access challenges remain but are related to distribution and cost, not supply.
HyperRAB is formulated at 300 IU/mL — twice the concentration of KedRAB and Imogam Rabies-HT (150 IU/mL). The dose is the same (20 IU/kg) but approximately half the volume is needed. When dilution is needed to increase wound infiltration volume, HyperRAB must be diluted with D5W (not normal saline). Carefully verify which product you have before calculating the dose.
Yes. HRIG may be administered up to and including Day 7 of the PEP series. However, it should never be given after Day 7, as the patient's antibody response to the vaccine is presumed to have occurred by that time, and HRIG administration may interfere with active immunity. Always start the vaccine series immediately regardless of HRIG availability.
All three HRIG manufacturers have patient assistance programs. Sanofi has historically supplied Imogam Rabies-HT at no charge to patients in need. Grifols (HyperRAB) can be reached at 1-800-520-2807 and Kedrion/Kamada (KedRAB) at 1-855-353-7466. State and county health departments may also be able to provide subsidized PEP for uninsured patients.
While no specific protective threshold for RVNA has been formally established by the FDA, the WHO has generally accepted a rabies virus neutralizing antibody (RVNA) titer of at least 0.5 IU/mL measured 14 days after initiation of PEP as protective. Titer testing is most important for immunocompromised patients or those on immunosuppressive therapy.
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