FDA LABEL RECORD
Icatibant
ICATIBANT. FDA prescribing information for this product, as published on the retrieval date below.
AS THE LABEL RECORDS IT
Product details
| Brand name | Icatibant |
|---|---|
| Generic name | ICATIBANT |
| Labeller | Alembic Pharmaceuticals Limited |
| Route | SUBCUTANEOUS |
| Label version | 1 |
| Effective | 2025-06-27 |
| Retrieved by this site | 2026-10-03 |
| Full label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8c149392-d281-4311-880f-3be2b4752f40 |
INDICATIONS AND USAGE
Quoted from the FDA label
1 INDICATIONS AND USAGE Icatibant injection is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adults 18 years of age and older. Icatibant injection is a bradykinin B2 receptor antagonist indicated for treatment of acute attacks of hereditary angioedema (HAE) in adults 18 years of age and older. ( 1 )
What this page is
A reproduction of a public FDA label record. Everything quoted above is the labeller's wording as published by the FDA, not this site's. Nothing here is regulatory, legal or medical advice, and a label being reproduced says nothing about whether a product is available in any particular country. Labels are revised often; the retrieval date above says when this copy was taken, and the full current label is at the link.
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