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Official Description

Hepatitis B immune globulin (HBIg), human, for intramuscular use

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 90371 refers to Hepatitis B immune globulin (HBIg), which is a human-derived immunizing agent administered via intramuscular injection. This product is a concentrated solution containing antibodies specifically designed to provide short-term, passive immunity against the hepatitis B virus. Unlike active immunization, where the recipient's immune system is stimulated to produce its own antibodies, HBIg offers immediate protection without triggering the body's immune response to generate additional antibodies. The antibodies present in HBIg are sourced from the pooled blood of multiple donors who have previously developed immunity to hepatitis B, ensuring a robust supply of protective antibodies. This code is specifically used to report the administration of human hepatitis B immune globulin for intramuscular use, focusing solely on the product itself rather than any associated procedures or services.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The administration of Hepatitis B immune globulin (HBIg) is indicated for specific clinical scenarios where immediate passive immunity is required to protect against hepatitis B infection. The following conditions warrant the use of HBIg:

  • Post-exposure prophylaxis for individuals who have been exposed to hepatitis B virus, particularly in cases of needlestick injuries or sexual exposure to an infected individual.
  • Prevention of hepatitis B infection in newborns born to mothers who are hepatitis B surface antigen (HBsAg) positive, ensuring that the infant receives immediate protection against the virus.
  • Immunocompromised patients who may not respond adequately to hepatitis B vaccination and require additional protection against potential exposure to the virus.

2. Procedure

The procedure for administering Hepatitis B immune globulin (HBIg) involves several key steps to ensure safe and effective delivery of the immunizing agent. The following procedural steps are outlined:

  • Step 1: Patient Assessment - Prior to administration, a thorough assessment of the patient’s medical history and potential exposure to hepatitis B virus is conducted. This includes evaluating the need for passive immunity based on the indications for HBIg use.
  • Step 2: Preparation of the HBIg - The HBIg solution is prepared according to the manufacturer's instructions. This may involve checking the expiration date, ensuring the integrity of the packaging, and drawing the appropriate dosage into a syringe while maintaining aseptic technique.
  • Step 3: Administration - The HBIg is administered via intramuscular injection, typically into the deltoid muscle for adults or the anterolateral thigh for infants. The injection site is cleaned with an antiseptic wipe to minimize the risk of infection, and the injection is performed using a sterile needle and syringe.
  • Step 4: Post-Administration Monitoring - After the injection, the patient is monitored for any immediate adverse reactions or side effects. This includes observing for signs of allergic reactions or local reactions at the injection site.

3. Post-Procedure

Following the administration of Hepatitis B immune globulin (HBIg), patients are typically advised to remain under observation for a short period to ensure there are no immediate adverse reactions. It is important to provide the patient with information regarding potential side effects, which may include mild pain or swelling at the injection site, fever, or allergic reactions. Patients should also be informed about the importance of follow-up care, especially if they are at risk for hepatitis B infection, and the need for additional vaccinations or treatments as recommended by their healthcare provider. Documentation of the administration, including the lot number of the HBIg, dosage, and injection site, should be recorded in the patient's medical record for future reference and compliance purposes.

Short Descr HEP B IG IM
Medium Descr HEPATITIS B IMMUNE GLOBULIN HBIG HUMAN IM
Long Descr Hepatitis B immune globulin (HBIg), human, for intramuscular use
Related Drugs HYPERHEP B
Status Code Excluded from Physician Fee Schedule by Regulation
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 9 - Not Applicable
Multiple Procedures (51) 9 - Concept does not apply.
Bilateral Surgery (50) 9 - Concept does not apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 9 - Concept does not apply.
Co-Surgeons (62) 9 - Concept does not apply.
Team Surgery (66) 9 - Concept does not apply.
Diagnostic Imaging Family 99 - Concept Does Not Apply
APC Status Indicator Nonpass-Through Drugs and Nonimplantable Biologicals, Including Therapeutic Radiopharmaceuticals
ASC Payment Indicator Drugs and biologicals paid separately when provided integral to a surgical procedure on ASC list; payment based on OPPS rate.
Type of Service (TOS) 1 - Medical Care
Berenson-Eggers TOS (BETOS) P6D - Minor procedures - other (non-Medicare fee schedule)
MUE 10
CCS Clinical Classification 228 - Prophylactic vaccinations and inoculations
JZ Zero drug amount discarded/not administered to any patient
59 Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25.
RT Right side (used to identify procedures performed on the right side of the body)
Date
Action
Notes
2011-01-01 Changed Short description changed.
1999-01-01 Added First appearance in code book in 1999.
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