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Billing and Coding: Intravenous Immunoglobulin (IVIG)

Medicare Coverage Database article A56718

Article

Contractor
Palmetto GBA
States (A/B MAC)
AL, GA, NC, SC, TN, VA, WV
Effective
Jul 1, 2026
Contractor numbers
10111, 10112, 10211, 10212, 10311, 10312, 11201, 11202, 11301, 11302, 11401, 11402, 11501, 11502
Read the article's coding instructions on CMS — which codes go together, documentation, and frequency limits — before billing. CodeRx lists the codes, not the instructions.

Drug codes in this article

HCPCS Level II drug codes the article lists (other codes it lists are not shown).

Covered ICD-10-CM codes (212)

Diagnosis codes the article lists as supporting medical necessity, grouped as in the article, with CMS's descriptions.

  • A85.8Other specified viral encephalitis
  • B08.3Erythema infectiosum [fifth disease]
  • B20Human immunodeficiency virus [HIV] disease
  • B25.0Cytomegaloviral pneumonitis
  • B25.1Cytomegaloviral hepatitis
  • B25.2Cytomegaloviral pancreatitis
  • B25.8Other cytomegaloviral diseases
  • B25.9Cytomegaloviral disease, unspecified
  • C88.00Waldenstrom macroglobulinemia not having achieved remission
  • C90.00Multiple myeloma not having achieved remission
  • C90.02Multiple myeloma in relapse
  • C91.10Chronic lymphocytic leukemia of B-cell type not having achieved remission
  • C91.11Chronic lymphocytic leukemia of B-cell type in remission
  • C91.12Chronic lymphocytic leukemia of B-cell type in relapse
  • D47.3Essential (hemorrhagic) thrombocythemia
  • D55.0Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
  • D55.1Anemia due to other disorders of glutathione metabolism
  • D55.21Anemia due to pyruvate kinase deficiency
  • D55.29Anemia due to other disorders of glycolytic enzymes
  • D55.3Anemia due to disorders of nucleotide metabolism
  • D55.8Other anemias due to enzyme disorders
  • D55.9Anemia due to enzyme disorder, unspecified
  • D56.0Alpha thalassemia
  • D56.1Beta thalassemia
  • D56.2Delta-beta thalassemia
  • D56.3Thalassemia minor
  • D56.4Hereditary persistence of fetal hemoglobin [HPFH]
  • D56.5Hemoglobin E-beta thalassemia
  • D56.8Other thalassemias
  • D56.9Thalassemia, unspecified
  • D57.00Hb-SS disease with crisis, unspecified
  • D57.01Hb-SS disease with acute chest syndrome
  • D57.02Hb-SS disease with splenic sequestration
  • D57.03Hb-SS disease with cerebral vascular involvement
  • D57.04Hb-SS disease with dactylitis
  • D57.09Hb-SS disease with crisis with other specified complication
  • D57.1Sickle-cell disease without crisis
  • D57.20Sickle-cell/Hb-C disease without crisis
  • D57.211Sickle-cell/Hb-C disease with acute chest syndrome
  • D57.212Sickle-cell/Hb-C disease with splenic sequestration
  • D57.213Sickle-cell/Hb-C disease with cerebral vascular involvement
  • D57.214Sickle-cell/Hb-C disease with dactylitis
  • D57.218Sickle-cell/Hb-C disease with crisis with other specified complication
  • D57.219Sickle-cell/Hb-C disease with crisis, unspecified
  • D57.3Sickle-cell trait
  • D57.414Sickle-cell thalassemia, unspecified, with dactylitis
  • D57.434Sickle-cell thalassemia beta zero with dactylitis
  • D57.454Sickle-cell thalassemia beta plus with dactylitis
  • D57.80Other sickle-cell disorders without crisis
  • D57.811Other sickle-cell disorders with acute chest syndrome
  • D57.812Other sickle-cell disorders with splenic sequestration
  • D57.813Other sickle-cell disorders with cerebral vascular involvement
  • D57.814Other sickle-cell disorders with dactylitis
  • D57.818Other sickle-cell disorders with crisis with other specified complication
  • D57.819Other sickle-cell disorders with crisis, unspecified
  • D58.0Hereditary spherocytosis
  • D58.1Hereditary elliptocytosis
  • D58.2Other hemoglobinopathies
  • D58.8Other specified hereditary hemolytic anemias
  • D58.9Hereditary hemolytic anemia, unspecified
  • D59.0Drug-induced autoimmune hemolytic anemia
  • D59.11Warm autoimmune hemolytic anemia
  • D59.12Cold autoimmune hemolytic anemia
  • D59.13Mixed type autoimmune hemolytic anemia
  • D59.9Acquired hemolytic anemia, unspecified
  • D61.01Constitutional (pure) red blood cell aplasia
  • D61.02Shwachman-Diamond syndrome
  • D61.810Antineoplastic chemotherapy induced pancytopenia
  • D61.811Other drug-induced pancytopenia
  • D61.818Other pancytopenia
  • D69.0Allergic purpura
  • D69.3Immune thrombocytopenic purpura
  • D69.41Evans syndrome
  • D69.42Congenital and hereditary thrombocytopenia purpura
  • D69.49Other primary thrombocytopenia
  • D80.0Hereditary hypogammaglobulinemia
  • D80.1Nonfamilial hypogammaglobulinemia
  • D80.2Selective deficiency of immunoglobulin A [IgA]
  • D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
  • D80.4Selective deficiency of immunoglobulin M [IgM]
  • D80.5Immunodeficiency with increased immunoglobulin M [IgM]
  • D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
  • D80.7Transient hypogammaglobulinemia of infancy
  • D80.8Other immunodeficiencies with predominantly antibody defects
  • D80.9Immunodeficiency with predominantly antibody defects, unspecified
  • D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
  • D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
  • D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
  • D81.4Nezelof's syndrome
  • D81.5Purine nucleoside phosphorylase [PNP] deficiency
  • D81.6Major histocompatibility complex class I deficiency
  • D81.7Major histocompatibility complex class II deficiency
  • D81.82Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
  • D81.89Other combined immunodeficiencies
  • D81.9Combined immunodeficiency, unspecified
  • D82.0Wiskott-Aldrich syndrome
  • D82.1Di George's syndrome
  • D82.2Immunodeficiency with short-limbed stature
  • D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
  • D82.4Hyperimmunoglobulin E [IgE] syndrome
  • D82.8Immunodeficiency associated with other specified major defects
  • D82.9Immunodeficiency associated with major defect, unspecified
  • D83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
  • D83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
  • D83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
  • D83.8Other common variable immunodeficiencies
  • D83.9Common variable immunodeficiency, unspecified
  • D84.0Lymphocyte function antigen-1 [LFA-1] defect
  • D84.1Defects in the complement system
  • D84.9Immunodeficiency, unspecified
  • D89.3Immune reconstitution syndrome
  • D89.810Acute graft-versus-host disease
  • D89.811Chronic graft-versus-host disease
  • D89.812Acute on chronic graft-versus-host disease
  • D89.813Graft-versus-host disease, unspecified
  • D89.82Autoimmune lymphoproliferative syndrome [ALPS]
  • D89.831Cytokine release syndrome, grade 1
  • D89.832Cytokine release syndrome, grade 2
  • D89.833Cytokine release syndrome, grade 3
  • D89.834Cytokine release syndrome, grade 4
  • D89.835Cytokine release syndrome, grade 5
  • D89.839Cytokine release syndrome, grade unspecified
  • D89.84IgG4-related disease
  • D89.89Other specified disorders involving the immune mechanism, not elsewhere classified
  • D89.9Disorder involving the immune mechanism, unspecified
  • G04.81Other encephalitis and encephalomyelitis
  • G11.3Cerebellar ataxia with defective DNA repair
  • G13.0Paraneoplastic neuromyopathy and neuropathy
  • G13.1Other systemic atrophy primarily affecting central nervous system in neoplastic disease
  • G25.82Stiff-man syndrome
  • G35.ARelapsing-remitting multiple sclerosis
  • G60.3Idiopathic progressive neuropathy
  • G61.0Guillain-Barre syndrome
  • G61.81Chronic inflammatory demyelinating polyneuritis
  • G61.82Multifocal motor neuropathy
  • G61.89Other inflammatory polyneuropathies
  • G62.81Critical illness polyneuropathy
  • G62.89Other specified polyneuropathies
  • G64Other disorders of peripheral nervous system
  • G70.00Myasthenia gravis without (acute) exacerbation
  • G70.01Myasthenia gravis with (acute) exacerbation
  • G70.80Lambert-Eaton syndrome, unspecified
  • G70.81Lambert-Eaton syndrome in disease classified elsewhere
  • G70.9Myoneural disorder, unspecified
  • G72.49Other inflammatory and immune myopathies, not elsewhere classified
  • G72.81Critical illness myopathy
  • G72.89Other specified myopathies
  • G73.1Lambert-Eaton syndrome in neoplastic disease
  • G73.3Myasthenic syndromes in other diseases classified elsewhere
  • H54.7Unspecified visual loss
  • L10.0Pemphigus vulgaris
  • L10.1Pemphigus vegetans
  • L10.2Pemphigus foliaceous
  • L10.3Brazilian pemphigus [fogo selvagem]
  • L10.4Pemphigus erythematosus
  • L10.5Drug-induced pemphigus
  • L10.81Paraneoplastic pemphigus
  • L10.89Other pemphigus
  • L10.9Pemphigus, unspecified
  • L12.0Bullous pemphigoid
  • L12.1Cicatricial pemphigoid
  • L12.8Other pemphigoid
  • L12.9Pemphigoid, unspecified
  • L13.8Other specified bullous disorders
  • L95.0Livedoid vasculitis
  • L95.9Vasculitis limited to the skin, unspecified
  • M30.3Mucocutaneous lymph node syndrome [Kawasaki]
  • M33.00Juvenile dermatomyositis, organ involvement unspecified
  • M33.01Juvenile dermatomyositis with respiratory involvement
  • M33.02Juvenile dermatomyositis with myopathy
  • M33.03Juvenile dermatomyositis without myopathy
  • M33.09Juvenile dermatomyositis with other organ involvement
  • M33.10Other dermatomyositis, organ involvement unspecified
  • M33.11Other dermatomyositis with respiratory involvement
  • M33.12Other dermatomyositis with myopathy
  • M33.13Other dermatomyositis without myopathy
  • M33.19Other dermatomyositis with other organ involvement
  • M33.20Polymyositis, organ involvement unspecified
  • M33.21Polymyositis with respiratory involvement
  • M33.22Polymyositis with myopathy
  • M33.29Polymyositis with other organ involvement
  • M33.90Dermatopolymyositis, unspecified, organ involvement unspecified
  • M33.91Dermatopolymyositis, unspecified with respiratory involvement
  • M33.92Dermatopolymyositis, unspecified with myopathy
  • M33.93Dermatopolymyositis, unspecified without myopathy
  • M33.99Dermatopolymyositis, unspecified with other organ involvement
  • M36.0Dermato(poly)myositis in neoplastic disease
  • M60.80Other myositis, unspecified site
  • R78.81Bacteremia
  • T86.10Unspecified complication of kidney transplant
  • T86.11Kidney transplant rejection
  • T86.12Kidney transplant failure
  • T86.13Kidney transplant infection
  • T86.19Other complication of kidney transplant
  • T86.21Heart transplant rejection
  • T86.22Heart transplant failure
  • T86.23Heart transplant infection
  • T86.298Other complications of heart transplant
  • T86.5Complications of stem cell transplant
  • Z41.8Encounter for other procedures for purposes other than remedying health state
  • Z48.21Encounter for aftercare following heart transplant
  • Z48.22Encounter for aftercare following kidney transplant
  • Z48.23Encounter for aftercare following liver transplant
  • Z48.24Encounter for aftercare following lung transplant
  • Z48.280Encounter for aftercare following heart-lung transplant
  • Z48.288Encounter for aftercare following multiple organ transplant
  • Z48.290Encounter for aftercare following bone marrow transplant
  • Z48.298Encounter for aftercare following other organ transplant
  • Z94.0Kidney transplant status
  • Z94.1Heart transplant status
  • Z94.81Bone marrow transplant status
  • Z94.84Stem cells transplant status

Disclaimer. This application provides informational coding and reimbursement reference data. It does not constitute legal, clinical, coding, or billing advice. Codes, payment amounts, payer rules, and coverage policies can change. Verify all information with current CMS publications, the applicable payer, and your organization’s compliance policies before submitting a claim. CodeRx is not affiliated with or endorsed by CMS, FDA, Medicare, or any payer.