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Ibrutinib 140mg Capsule

Anti Cancer Medicines WHO-GMP Certified
Anti Cancer Medicines

Ibrutinib 140mg Capsule

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Product Details

Packaging
Box (30 capsules)
Strength
140 mg
Brand
Nitib
Manufacturer
Hetero
Form
Capsule

Description

IBRUTINIB as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL). IBRUTINIB as a single agent or in combination with rituximab or obinutuzumab is indicated for the treatment of adult patIMBRUVICA as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL). IBRUTINIB as a single agent or in combination with rituximab or obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL) (see section 5.1). IBRUTINIB as a single agent or in combination with bendamustine and rituximab (BR) is indicated for the treatment of adult patients with CLL who have received at least one prior therapy. IBRUTINIB as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL). IBRUTINIBas a single agent or in combination with rituximab or obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL) (see section 5.1). IBRUTINIB as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL). IBRUTINIBas a single agent or in combination with rituximab or obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL) (see section 5.1). IBRUTINIB as a single agent or in combination with bendamustine and rituximab (BR) is indicated for the treatment of adult patients with CLL who have received at least one prior therapy. IBRUTINIB as a single agent is indicated for the treatment of adult patients with Waldenström's macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. IMBRUVICA in combination with rituximab is indicated for the treatment of adult patients with WM. as a single agent or in combination with bendamustine and rituximab (BR) is indicated for the treatment of adult patients with CLL who have received at least one prior therapy. IBRUTINIB as a single agent is indicated for the treatment of adult patients with Waldenström's macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. IMBRUVICA in combination with rituximab is indicated for the treatment of adult patients with WM. as a single agent is indicated for the treatment of adult patients with Waldenström's macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. IMBRUVICA in combination with rituximab is indicated for the treatment of adult patients with WM.ients with previously untreated chronic lymphocytic leukaemia (CLL) (see section 5.1). IBRUTINIB as a single agent or in combination with bendamustine and rituximab (BR) is indicated for the treatment of adult patients with CLL who have received at least one prior therapy. IBRUTINIBas a single agent is indicated for the treatment of adult patients with Waldenström's macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. IMBRUVICA in combination with rituximab is indicated for the treatment of adult patients with WM.


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