Alembic Pharmaceuticals receives USFDA approval for its generic Icatibant injection for treating hereditary angioedema.

Alembic Pharmaceuticals receives USFDA approval for its generic Icatibant injection, used to treat acute attacks of hereditary angioedema (HAE) in adults. This is the company's first peptide product approval and the estimated market size for the injection is $112 million for the 12 months ending Mar 2024. The approved ANDA is therapeutically equivalent to Takeda Pharmaceuticals U.S.A., Inc.'s Firazyr Injection.

June 17, 2024
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