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colistimethate sodium

Powder for solution for injection 1 IU, 2 IU, 3 IU, 4.5 IU

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Unavailable markets
Vietnam
Manufacturer #35915

Established in 2007, this family-owned manufacturer specializes in pharmaceutical formulations, offering over 500 products across various dosage forms, including tablets, capsules, dry syrups, ointments, dry injections, and liquid orals. As a CTD dossier owner and manufacturer, it holds WHO-cGMP certification, ensuring compliance with stringent international quality standards. The manufacturer operates advanced production lines with capacities such as 3,600 million tablets, 1,800 million capsules, 240 million liquid injections in ampoules, and 70 million dry powder injections per annum, adhering to rigorous GMP guidelines. As a CTD dossier owner and manufacturer, its products are distributed across multiple countries worldwide.

Manufacturer usually replies in 7 days

colistimethate sodium

Powder for solution for injection 150 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO, EU GMP
Manufacturer #20273
A pharmaceutical manufacturer specializing in contract research and development as well as formulation services for pharmaceutical products including solid orals, injectables, liquids, ophthalmics and complex/niche dosage forms. The company offers comprehensive services spanning pre-formulation, formulation development, analytical method development and validation, stability testing, bioequivalence support, dossier preparation, and regulatory-filing assistance — enabling partners to take products from development through to commercialization under globally accepted standards. Their facilities are described as compliant with USFDA/EU-approved manufacturing requirements, supporting development of both generic and specialized pharmaceutical products for global markets.

Manufacturer usually replies in 14 days

colistimethate sodium

Injection 1 IU, 2 IU, 3 IU, 4.5 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #36197

Established in 2018, this manufacturer specializes in exporting and manufacturing pharmaceutical active pharmaceutical ingredients (APIs) and finished formulations, including tablets, capsules, pre-filled syringes, dry syrups, creams, ointments, injectables (liquids and powder), eye/ear drops, IV fluids, and surgical products. As a CTD dossier owner and manufacturer, it holds EU/WHO GMP certifications, ensuring compliance with international quality standards. The manufacturer operates advanced production lines adhering to stringent GMP guidelines. As a CTD dossier owner and manufacturer, its products are distributed across various regions, including Central America, non-EU Europe, the Middle East, Oceania, South America, and South Asia.

Manufacturer usually replies in 77 days

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Colistimethate Sodium

Colistimethate Sodium is an antibiotic derived from bacteria of the genus Paenibacillus. It is the last- resort treatment for multidrug-resistant Gram-negative infections including pneumonia which includes infections caused by Pseudomonas aeruginosa, Klebsiella pneumoniae, or Acinetobacter. Colistimethate Sodium is supplied in forms for injection into a vein or into a muscle, or inhaled, known as Colistimethate sodium and can also be applied to the skin or taken by mouth, known as colistin sulfate. Colistimethate Sodium is sold under the brand names Xylistin, Coly-Mycin M, Colobreathe among others. Koyama discovered polymyxins, initially in 1947, and Colistimethate Sodium as a secondary metabolite of the Gram-positive soil. It was approved for medical use in the United States in 1970. Due to its safety record and worldwide use, it features on the World Health Organization's List of Essential Medicines in addition to classifying Colistimethate Sodium as critically important for human medicine. Since the expiry of its initial patent protection, it is now made by several companies around the world as a generic medication.

Dosage Forms & Administration

Colistimethate Sodium is sold as a powder for injection in 150mg per vial. In the treatment of Susceptible Infections, the initial adult dose prescribed is 2.5-5 mg per kilo per day, spaced 6 to 12 hours apart. The daily maximum dose can not exceed 5 mg. this is followed by a Maintenance dose of 9MIU a day, administered in 2-3 divided doses and for critically ill patients, an initial loading dose of 9 MIU is prescribed.

The price of Colistimethate Sodium

In India, the consumers have to pay a retail price of USD 600 for a supply of 60 vials of generic brand of 1 MIU Colistimethate Sodium injection. This price is significantly higher in the developed world. In the USA, a generic brand supply of 60 vials of 150mg costs the consumer an average retail price of $2,883.38.

How does Colistimethate Sodium?

Colistimethate is an anti-biotic and also acts as a surface-active agent. It penetrates into and disrupts the bacterial cell membrane. Colistimethate has both hydrophobic and lipophilic moieties as a polycationic. It interacts and changes the permeability of the bacterial cytoplasmic membrane leading to the deal of bacteria cells.

Finding Colistimethate Sodium Manufacturers and Suppliers

The best way to find and gain access to Colistimethate Sodium manufacturers and Colistimethate Sodium suppliers are to make through Pipelinepharma's global B2B online marketplace for medicines and other pharmaceuticals. Normally, finding trusted manufacturers and supplies of specific drugs like Colistimethate Sodium can be a time-consuming challenge, but with Pipelinepharma's simple search engine and network of proven partners, the whole process becomes a lot easier. All you need to do to get started is to make use of our integrated search engine and start looking for suppliers or manufacturers of Colistimethate Sodium to work with. You can fine-tune your search results using various filters too, letting you search for Colistimethate Sodium from specific countries.

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