for oral use Initial U.S. Approval: YYYY
Lytgobi (futibatinib) is a kinase inhibitor indicated for the treatment of adult patients with previously treated, unresectable, locally advanced or metastatic intrahepatic cholangiocarcinoma harboring fibroblast growth factor receptor 2 (FGFR2) gene fusions or other rearrangements. This medicine was approved by the FDA in the USA on 22 September 2022.
Facts about futibatinib) tablets
Approval Date: 9/30/2022
Proprietary Name: Lytgobi
Active Ingredient(s): futibatinib
DISEASE INDICATIONS-Bile Duct Cancer
USAGE-Tablets: 4 mg
MEDICINE APPROVED BY-Food and Drug Administration (FDA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “futibatinib) tablets” based on the information you provide.
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Query For futibatinib tablets
Approved accessible "futibatinib tablets"
Futibatinib, is a medication used for the treatment of cholangiocarcinoma (bile duct cancer). It is a kinase inhibitor. Futibatinib was approved for medical use in the United States in September 2022.
Futibatinib is indicated for the treatment of adults with previously treated, unresectable, locally advanced or metastatic intrahepatic cholangiocarcinoma harboring fibroblast growth factor receptor 2 (FGFR2) gene fusions or other rearrangements.
How can 1 go about obtaining futibatinib tablets?
If futibatinib tablets are not yet approved or available in your area, you may request its price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).
Lytgobi (futibatinib tablets) for oral use Initial U.S. Approval: YYYY
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