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Country of origin : Iceland

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1 products found

ponatinib

Tablets, film coated 15 mg, 30 mg, 45 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
Iceland
GMP approvals
EU GMP
Manufacturer #28915
This company specializes in generic pharmaceuticals within the EU region. They offer out-licensing and contract manufacturing services to pharmaceutical companies seeking high-quality production from a reliable European partner. Their facility utilizes green energy sources, highlighting their commitment to sustainability. While specific therapy areas and product details are not provided, they likely focus on various dosage forms common in generic pharmaceuticals. The company emphasizes its skilled workforce and dedication to employee well-being.

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Ponatinib Manufacturer

Ponatinib is available under the brand name “Iclusig”. It belongs to the drug class of Antineoplastic and Tyrosine Kinase Inhibitor”. It is indicated for the treatment of adults with chronic, accelerated, or blast-phase chronic myeloid leukemia (CML) that is resistant or intolerant to prior tyrosine kinase inhibitor therapy, or Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) that is resistant or intolerant to prior tyrosine kinase inhibitor therapy. This pharmaceutical medicine can be taken with or without a meal. In case of a missed dose, take the next scheduled dose the following day. Storing at a temperature of 20-25oC (68-77oF); excursions to 15-30oC are permitted. The most common non-hematologic adverse reactions related to this pharmaceutical medicine include hypertension, rash, abdominal pain, dry skin, constipation, arthralgia, and pyrexia. The hematologic adverse reactions include thrombocytopenia, anaemia, neutropenia, lymphopenia, and leukopenia. Your doctor or pharmacist should be informed of your medical history before you take this medicine, especially if you have: liver disease; heart problems (such as angina; high blood pressure); a previous stroke or mini-stroke (transient ischemic attack); diabetes; high cholesterol; and tobacco use. Verify the pregnancy status of females of reproductive potential before beginning the procedure. There is no information on the drug's presence in human milk, its effects on breastfed infants, or its effects on milk production. Women should not breastfeed during treatment and for 6 days after the last dose U.S. Food and Drug Administration has approved Ponatinib for adults with chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL).

How does Ponatinib work?

Ponatinib is a kinase inhibitor with multiple targets. There is a constitutively active protein in CML known as Bcr-Abl. It inhibits Abl and T315I mutant kinase tyrosine kinase activity. Due to its ability to block the binding of Bcr-Abl inhibitors, the T315I mutation confers resistance in cells.

The cost of Ponatinib

A 30-tablet supply of Ponatinib oral tablet 10 mg costs approximately $18,711, depending on the pharmacy you visit.

Sourcing the Ponatinib Manufacturer and Suppliers

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Pipelinepharma is a global online marketplace. It is structured to simplify pharmaceutical deals by providing its customers with an intuitive interface that is easy to engage with. The Ponatinib manufacturers and suppliers list can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. These advanced filters can also filter out the countries for this medicine’s manufacturers and suppliers. These also enable you to check the dossier status of this medicine, and the GMP approvals of the different variants of Ponatinib. Each manufacturer or supplier product description contains essential information about this substance including clinical data, stability zones, countries where Ponatinib is manufactured in

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