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Capecitabine manufacturers

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Country of origin : Argentina

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6 products found

capecitabine

Tablets 500 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Argentina
GMP approvals
WHO
Manufacturer #15160
This pharmaceutical company specializes in the production of oncological medications, including both oral solids and injectables. Their state-of-the-art manufacturing facility adheres to strict GMP standards for quality control and produces a range of products covering various oncology therapy areas. They operate globally with a presence in over 15 countries across regions like North America and the EU. The company prioritizes research and development, constantly seeking new formulations and improving existing ones. They hold multiple certifications and are committed to ensuring the safety, efficacy, and accessibility of their oncological medications.

Manufacturer usually replies in 5 days

capecitabine

Tablets 500mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Argentina
GMP approvals
PICS
Unavailable markets
Costa Rica
Manufacturer #678
It is situated in the southern part of South America. It is committed to excellence and continuous improvement. They have a production plant for the manufacturing of high value-added products like the treatment of HIV-AIDS and neurodegenerative and cardiovascular diseases.

Manufacturer usually replies in 3 days

capecitabine

Tablets 500 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Argentina
GMP approvals
PICS
Manufacturer #16454
A pharmaceutical company based in South America with 15+ years of experience in a drug market. More than 40 products in 25+ countries: LATAM; Wester, Southern and South-eastern Asia. Company’s therapeutic areas consist of products that can used in such areas as: urology, oncology, rare diseases and more.

Manufacturer usually replies in 7 days

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Capecitabine Manufacturers

Capecitabine belongs to the class antimetabolite that goes by the brand name Xeloda in the market. Capecitabine Manufacturers is a fluoropyrimidine carbamate with antineoplastic action used for the therapy of metastatic bosom malignancy and colon disease. Capecitabine is contraindicated in patients with serious renal impedance hypersensitivity, ones who show allergic reactions to capecitabine or to any of its segments, and to 5-fluorouracil. Some of the common side effects that are experienced in approximately 30% (or more) of patients can include weakness and fatigue during the treatment and after the treatment, poor appetite, diarrhea, mouth sores, feeling nauseous and abdominal pain. The less common side effects include symptoms such as; low platelet count, fever, eye irritation, constipation, swelling of feet and ankles, gastrointestinal motility disorders, and some more. The route of administration for this pharmaceutical remedy is an oral route and is usually taken after 30 minutes of having a meal, with water. The daily dose given depends on many components, that can be the height and weight of the patient, other comorbidities, the severity of the disease, etc. Capecitabine Manufacturers have been approved for medical use by FDA in 1998 and fall in the World Health Organization's List of Essential Medicines. This pharmaceutical medicine can cause fetal damage when regulated to a pregnant lady. Advise pregnant ladies about the possible danger to an embryo. Prompt females not to breastfeed during treatment with Capecitabine and for about fourteen days after the last portion. Capecitabine is an antitumor fluoropyrimidine carbamate that is used to cure metastatic melanoma and colorectal cancer. It's a systemic prodrug given orally that has minimal pharmacologic action until it's transformed to fluorouracil by kinases found in higher doses in various cancers. Fluorouracil was then converted to 5-fluoro-2′-deoxyuridine 5′-monophosphate (FdUMP) and 5-fluorouridine triphosphate for both normal and malignant cells (FUTP).

How Does Capecitabine Work?

Capecitabine is a dehydrogenase inhibitor. Capecitabine is converted by the body into fluorouracil, a common chemotherapy medication. Fluorouracil instructs cells to stop producing and repairing DNA. In order to thrive and grow, diseased cells must create and repair DNA. Capecitabine is a pro-drug that is converted to its cytotoxic component, fluorouracil, by the enzyme thymidine phosphorylase, which is present in higher amounts in many cancers than in body cells or plasma. Fluorouracil has been further converted in normal and cancerous cells to 2 existing metabolites, 5-fluoro-2'-deoxyuridine 5'-monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP). Two processes are involved in the cell damage caused by these compounds. FdUMP and the folic cofactor, N5-10-methylenetetrahydrofolate, first create a covalently bonded ternary complex with thymidylate synthase (TS). This interaction prevents 2'-deaxyuridylate from becoming thymidylate. Because thymidylate is a crucial precursor of tyrosine triphosphate, which is required for DNA synthesis, a lack of this chemical can prevent cell division. Second, as during the production of RNA, nuclear transcriptional enzymes may incorrectly include FUTP instead of uridine triphosphate (UTP). Through the generation of counterfeit RNA, this metabolic mistake can disrupt RNA processing and protein synthesis. The majority of capecitabine and its metabolic products are excreted in the urine; 95.5 percent of the capecitabine therapeutic dose is recovered in urine. The amount of feces excreted is little (2.6 percent ). FBAL, which accounts for 57 percent of the injected drug, is the most common metabolite eliminated in urine. About 3% of the given dose is eliminated unaltered in the urine.

The Wholesale Price of Capecitabine

This drug can be purchased at any drugstore. It is also available in online mode for sale. TheWholesalecost for capecitabine oral tablet 500 mg is around $111 for a stock of 120 tablets, which can vary, depending upon the drug store you visit. Per unit, the cost is $0.58 – $10.40. Costs are only applicable for cash purchasing consumers and do not apply to insurance programs. Pharmaceutical corporations and distributors generally support patient assistance programs (PAPs), which provide free or subsidized drugs to low-income, unemployed, or under-insured individuals who meet certain conditions.

Navigating Our Pharmaceutical Marketplace

Being a global B2B pharmaceutical online marketplace, Pipelinepharma is structured to simplify pharmaceutical deals by providing you with an intuitive interface that is easy to engage with. The selection of Capecitabine Manufacturer’s and distributors offerings can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. The advanced filters help you filter out the countries for these substance manufacturers and Capecitabine suppliers that you are looking for. These also enable you to check the dossier status of this medicine, and the GMP approvals of the different variants of Capecitabine Manufacturers Also, each manufacturer or Capecitabine suppliers product description contains essential information about this substance including clinical data, stability zones, countries where CapecitabineManufacturers is already registered in. Manufacturers also have special, and delivery terms.

Establishing Commercial Ties

Pipelinepharma presents a B2B commercial center where drug merchants, purchasers, and wholesalers are permitted to market or purchase drugs. Individuals holding a permit of medications can enroll themselves and publicize as many prescriptions as they need, or they can interface with a medication selling company via looking or offering tertiary support to the purchasers directly.

Quality Assurance

Pipelinepharma is a legitimate service platform. The site thoroughly verifies the pharmaceutical product's quality, duration of use, and seller information. To provide a safe and secure service to users, all pharmaceutical substances are first investigated thoroughly for any suspected defects before being promoted for marketing, and seller details are assessed during the registration process.

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