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  • TABLET;ORAL - 100MG
  • TABLET;ORAL - 25MG
  • TABLET;ORAL - 50MG
  • TABLET;ORAL - 12.5MG;100MG
  • TABLET;ORAL - 12.5MG;50MG
  • TABLET;ORAL - 25MG;100MG

Looking for 124750-99-8 / Losartan Potassium API manufacturers, exporters & distributors?

Losartan Potassium manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Losartan Potassium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Losartan Potassium manufacturer or Losartan Potassium supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Losartan Potassium manufacturer or Losartan Potassium supplier.

PharmaCompass also assists you with knowing the Losartan Potassium API Price utilized in the formulation of products. Losartan Potassium API Price is not always fixed or binding as the Losartan Potassium Price is obtained through a variety of data sources. The Losartan Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Losartan Potassium

Synonyms

124750-99-8, Cozaar, Erythropoietin, Losartan potassium salt, Lorzaar, Losacar

Cas Number

124750-99-8

Unique Ingredient Identifier (UNII)

3ST302B24A

About Losartan Potassium

An antagonist of ANGIOTENSIN TYPE 1 RECEPTOR with antihypertensive activity due to the reduced pressor effect of ANGIOTENSIN II.

Losartan Potassium Manufacturers

A Losartan Potassium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Losartan Potassium, including repackagers and relabelers. The FDA regulates Losartan Potassium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Losartan Potassium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Losartan Potassium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Losartan Potassium Suppliers

A Losartan Potassium supplier is an individual or a company that provides Losartan Potassium active pharmaceutical ingredient (API) or Losartan Potassium finished formulations upon request. The Losartan Potassium suppliers may include Losartan Potassium API manufacturers, exporters, distributors and traders.

click here to find a list of Losartan Potassium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Losartan Potassium USDMF

A Losartan Potassium DMF (Drug Master File) is a document detailing the whole manufacturing process of Losartan Potassium active pharmaceutical ingredient (API) in detail. Different forms of Losartan Potassium DMFs exist exist since differing nations have different regulations, such as Losartan Potassium USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Losartan Potassium DMF submitted to regulatory agencies in the US is known as a USDMF. Losartan Potassium USDMF includes data on Losartan Potassium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Losartan Potassium USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Losartan Potassium suppliers with USDMF on PharmaCompass.

Losartan Potassium JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Losartan Potassium Drug Master File in Japan (Losartan Potassium JDMF) empowers Losartan Potassium API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Losartan Potassium JDMF during the approval evaluation for pharmaceutical products. At the time of Losartan Potassium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Losartan Potassium suppliers with JDMF on PharmaCompass.

Losartan Potassium KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Losartan Potassium Drug Master File in Korea (Losartan Potassium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Losartan Potassium. The MFDS reviews the Losartan Potassium KDMF as part of the drug registration process and uses the information provided in the Losartan Potassium KDMF to evaluate the safety and efficacy of the drug.

After submitting a Losartan Potassium KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Losartan Potassium API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Losartan Potassium suppliers with KDMF on PharmaCompass.

Losartan Potassium CEP

A Losartan Potassium CEP of the European Pharmacopoeia monograph is often referred to as a Losartan Potassium Certificate of Suitability (COS). The purpose of a Losartan Potassium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Losartan Potassium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Losartan Potassium to their clients by showing that a Losartan Potassium CEP has been issued for it. The manufacturer submits a Losartan Potassium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Losartan Potassium CEP holder for the record. Additionally, the data presented in the Losartan Potassium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Losartan Potassium DMF.

A Losartan Potassium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Losartan Potassium CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Losartan Potassium suppliers with CEP (COS) on PharmaCompass.

Losartan Potassium WC

A Losartan Potassium written confirmation (Losartan Potassium WC) is an official document issued by a regulatory agency to a Losartan Potassium manufacturer, verifying that the manufacturing facility of a Losartan Potassium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Losartan Potassium APIs or Losartan Potassium finished pharmaceutical products to another nation, regulatory agencies frequently require a Losartan Potassium WC (written confirmation) as part of the regulatory process.

click here to find a list of Losartan Potassium suppliers with Written Confirmation (WC) on PharmaCompass.

Losartan Potassium NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Losartan Potassium as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Losartan Potassium API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Losartan Potassium as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Losartan Potassium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Losartan Potassium NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Losartan Potassium suppliers with NDC on PharmaCompass.

Losartan Potassium GMP

Losartan Potassium Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Losartan Potassium GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Losartan Potassium GMP manufacturer or Losartan Potassium GMP API supplier for your needs.

Losartan Potassium CoA

A Losartan Potassium CoA (Certificate of Analysis) is a formal document that attests to Losartan Potassium's compliance with Losartan Potassium specifications and serves as a tool for batch-level quality control.

Losartan Potassium CoA mostly includes findings from lab analyses of a specific batch. For each Losartan Potassium CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Losartan Potassium may be tested according to a variety of international standards, such as European Pharmacopoeia (Losartan Potassium EP), Losartan Potassium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Losartan Potassium USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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