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Lenalidomide manufacturers

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Country of origin : Turkey

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5 products found

lenalidomide

Capsules 5 mg, 10 mg, 15 mg, 25 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP, PICS
Manufacturer #2760
This pharmaceutical company, founded in 1991, specializes in developing and distributing prescription medications across key therapy areas like oncology, hematology, ophthalmology, and radiology. They are known for their commitment to providing innovative treatments, particularly for rare diseases (orphan drugs), often partnering with leading companies in the EU and North America for distribution within these regions. They prioritize high-quality products and ethical practices, maintaining GMP certifications and securing product patents. Their dosage forms encompass a range of prescription medications, reflecting their focus on precision medicine and addressing specific patient needs.

Manufacturer usually replies in 5 days

lenalidomide

Capsules 5 mg, 10 mg, 15 mg, 25 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP
Unavailable markets
Colombia , Mexico
Manufacturer #2722
It originally entered the pharmaceutical industry in 1987, when it introduced blood derivative products to Europe and became the exclusive distributor for prominent European brands. Oncology, hematology, dermatology, radiology, rheumatology, immunology, and OTC products are the seven main therapeutic fields.

lenalidomide

Capsules 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP
Registered in
Germany , Netherlands , Switzerland , Turkey
Comments
Reference product: Revlimid/Bristol-Myers Squibb
Manufacturer #13072
This pharmaceutical company, established in 1958, boasts a long history and operates across multiple regions, including Europe and North America. They specialize in the production of prescription medications, with a focus on three key therapy areas: oncology, immunology, and dermatology. Their principal dosage forms include tablets, capsules, and topical solutions. The company possesses GMP certifications and holds patents for several product innovations. With three production facilities and a logistics center, they prioritize efficiency and international expansion, aiming to become a global leader in the pharmaceutical industry.

Manufacturer usually replies in 29 days

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LENALIDOMIDE manufacturer

Lenalidomide is being sold under the trade names “Revlimid” and “Linamide”, and belongs to the class of immunomodulatory agents. It is commonly used in combination with Dexamethasone to treat Multi Myeloma (MM) mostly in adult patients. It is also used in maintenance therapy for Autologous Hematopoietic Stem Cell transplantation (auto-HSCT), transfusion-dependent Anemia due to low MDS (Myelodysplastic Syndromes), Mantle Cell Lymphoma (MCL) if the disease relapses after two therapies, and for previously treated Follicular Lymphoma (FL) or Marginal Zone Lymphoma (MZL) in combination therapy with Rituximab. Side effects related to this pharmaceutical medicine include pneumonia, upper respiratory tract infections, urinary tract infections, neutropenia, thrombocytopenia, anemia, arthralgia, asthenia, back pain, constipation, dizziness, vomiting, dyspnea, headache, fatigue, anorexia, hypokalemia, nasopharyngitis, edema, skin rash and xeroderma, and many more. Lenalidomide is contraindicated in patients who are suffering from conditions like; Hodgkin’s lymphoma, overactive thyroid gland, and low platelets count. This pharmaceutical remedy should be taken orally approximately at the same time each day, with or without food. This drug is not recommended during pregnancy as it causes severe and life-threatening birth defects or even death. It is also not recommended for nursing mothers. The FDA, on May 28, 2019, has approved Lenalidomide for the treatment of follicular and marginal zone lymphoma in combination with Rituximab. Warnings: Follow all Instructions on your medicine package and label. It is wise to tell your healthcare providers about all your medical allergies, illnesses, and all medicines you use. Before taking LENALIDOMIDE: You should not use This medical remedy if you are allergic to it This drug may also be used for purposes that may not have been listed in this medication guide.

How Does LENALIDOMIDE Work?

Lenalidomide has several mechanisms of action. One common mechanism is that it inhibits the proliferation and induces apoptosis of tumor cells, thus, showing anti-tumor effects.

How to use LENALIDOMIDE?

Read the LENALIDOMIDE Guide and, if available, the Patient Information Leaflet that will be provided by your pharmacist before you start taking LENALIDOMIDE. If you have any questions related to LENALIDOMIDE, ask your pharmacist or doctor. Take this medical remedy by mouth with or without food as instructed by your Health care professionals, usually once daily. Swallow this drug whole with water. For curing certain conditions, you may be directed to take this remedy in cycles (once daily for 21 days, then stop the remedy for 7 days). It is advised not open, chew, or break the capsules, or handle them any more than needed. If any of the powder from the capsule gets in touch with your skin, wash the area with soap and water. Use this medication regularly to get the most benefit from it. To help you remember, take it at the same time(s) each day. Keep taking this medication even if you feel well. Most people with high blood pressure do not feel sick. Tell your doctor if you do not get better or if you get worse.

How much money does LENALIDOMIDE cost?

The bulk supply of 28 capsules of Lenalidomide manufacturer of 2.5mg costs around $23,317.

Working with LENALIDOMIDE Manufacturers and LENALIDOMIDE Suppliers

If you are looking to find manufacturers and suppliers of LENALIDOMIDE, locate them quickly using Pipelinepharma's online marketplace. With this convenient B2B platform, you can order types of medications and quantities you require from companies that have passed our stringent vetting and quality control procedures.

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 LENALIDOMIDE 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 LENALIDOMIDE manufacturers and LENALIDOMIDE suppliers that you are looking for. These also enable you to check the dossier status of LENALIDOMIDE, and the GMP approvals of the different variants of LENALIDOMIDE. Also, each manufacturer or supplier product description contains essential information about LENALIDOMIDE including clinical data, stability zones, countries where LENALIDOMIDE is already registered in. Manufacturers also have special, and delivery terms.

Establishing commercial ties

If you are a pharmaceutical licensing company or a distributor you can enter into deals or negotiations over LENALIDOMIDE offers with manufacturing companies after completing the free registration process and joining our online marketplace. This helps to ensure that you conclude the pharmaceutical deal at a reasonable cost and achieve the best cost/benefit ratio for your company while bypassing lengthy sourcing, negotiation, and ordering process. Once you have finalized a deal, you can look forward to a long-lasting business relationship with the manufacturers or suppliers. This way, the marketplace allows you as a distributor to skip the process of shortlisting product manufacturers every time you are looking for in-licensing or distribution deals.

Quality Assurance

To keep up to the quality standards other than Good Manufacturing Practice approvals that LENALIDOMIDE manufacturers have, we qualify their companies before they are onboarded on the platform. This allows us to screen LENALIDOMIDE manufacturers for the quality of the pharmaceutical products’ dossiers and protect against the risk of possible malpractices.

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