J84.112
BillableIdiopathic pulmonary fibrosis
J84.112 is the ICD-10-CM code for Idiopathic pulmonary fibrosis. It is a billable, specific code valid for reimbursement.
J00-J99 Diseases of the respiratory system
What this means — in plain language
MedlinePlus · NIHPulmonary fibrosis is a condition in which the tissue deep in your lungs becomes scarred over time. This tissue gets thick and stiff. That makes it hard for you to catch your breath, and your blood may not get enough oxygen. Causes of pulmonary fibrosis include environmental pollutants, some medicines, some connective tissue diseases, and interstitial lung disease. Interstitial lung disease is the name for a large…
Read more about Pulmonary Fibrosis at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Includes
- •Cryptogenic fibrosing alveolitis
- •Idiopathic fibrosing alveolitis
Medications indicated for this condition
FDA labeling- TocilizumabInterleukin-6 Receptor Antagonist [EPC]›
- Nintedanib›
- PirfenidonePyridone [EPC]›
- CorticotropinAdrenocorticotropic Hormone [EPC]›
- Pirfenidone Capsule, 267 MgPyridone [EPC]›
Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.
Conditions mapped to this code
MedlinePlus · NIHPlain-language health-topic references grounded in MedlinePlus (NIH/NLM).
Frequently asked questions
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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