What strengths and dosage forms of METHOTREXATE are listed?

METHOTREXATE bulk supplier for pharma manufacturers

Methotrexate 150 mg Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 150 mg

Reference Brands:

Category: Arthritis

Injection contains methotrexate. It is used to treat severe psoriasis, and rheumatoid arthritis. In higher doses, methotrexate is used to treat cancer. Psoriasis is a skin disease that causes red, scaly patches, most commonly on the knees, elbows, and scalp. Arthritis is tenderness and swelling of one or more joints.

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Product Description: Talk to your doctor if you have gastrointestinal disorders, liver problems, kidney problems, vaccinated recently, build-up of fluid in the lining of lungs or abdomen, infection, or if you are receiving radiotherapy before taking this medicine. Talk to your doctor if you are on a salt-controlled diet.

Methotrexate — third party manufacturing & bulk supply

Methotrexate 150 mg is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.

Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.

Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Methotrexate is supplied as Injection — an injectable dosage form, so the indicative MOQ is 50,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.

Manufacturers of Methotrexate listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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