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PharmaCompass offers a list of Betahistine Dihydrochloride 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 Betahistine Dihydrochloride manufacturer or Betahistine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betahistine Dihydrochloride manufacturer or Betahistine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Betahistine Dihydrochloride API Price utilized in the formulation of products. Betahistine Dihydrochloride API Price is not always fixed or binding as the Betahistine Dihydrochloride Price is obtained through a variety of data sources. The Betahistine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Betahistine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betahistine, including repackagers and relabelers. The FDA regulates Betahistine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betahistine 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 Betahistine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Betahistine supplier is an individual or a company that provides Betahistine active pharmaceutical ingredient (API) or Betahistine finished formulations upon request. The Betahistine suppliers may include Betahistine API manufacturers, exporters, distributors and traders.
click here to find a list of Betahistine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Betahistine DMF (Drug Master File) is a document detailing the whole manufacturing process of Betahistine active pharmaceutical ingredient (API) in detail. Different forms of Betahistine DMFs exist exist since differing nations have different regulations, such as Betahistine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Betahistine DMF submitted to regulatory agencies in the US is known as a USDMF. Betahistine USDMF includes data on Betahistine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Betahistine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Betahistine suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Betahistine Drug Master File in Korea (Betahistine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Betahistine. The MFDS reviews the Betahistine KDMF as part of the drug registration process and uses the information provided in the Betahistine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Betahistine 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 Betahistine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Betahistine suppliers with KDMF on PharmaCompass.
A Betahistine CEP of the European Pharmacopoeia monograph is often referred to as a Betahistine Certificate of Suitability (COS). The purpose of a Betahistine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Betahistine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Betahistine to their clients by showing that a Betahistine CEP has been issued for it. The manufacturer submits a Betahistine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Betahistine CEP holder for the record. Additionally, the data presented in the Betahistine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Betahistine DMF.
A Betahistine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Betahistine 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 Betahistine suppliers with CEP (COS) on PharmaCompass.
A Betahistine written confirmation (Betahistine WC) is an official document issued by a regulatory agency to a Betahistine manufacturer, verifying that the manufacturing facility of a Betahistine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Betahistine APIs or Betahistine finished pharmaceutical products to another nation, regulatory agencies frequently require a Betahistine WC (written confirmation) as part of the regulatory process.
click here to find a list of Betahistine suppliers with Written Confirmation (WC) on PharmaCompass.
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 Betahistine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Betahistine API and other APIs are published in this directory by the FDA.
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 Betahistine 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.
The NDC directory also contains data on finished compounded human drug products that contain Betahistine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Betahistine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Betahistine suppliers with NDC on PharmaCompass.
Betahistine 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 Betahistine 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 Betahistine GMP manufacturer or Betahistine GMP API supplier for your needs.
A Betahistine CoA (Certificate of Analysis) is a formal document that attests to Betahistine's compliance with Betahistine specifications and serves as a tool for batch-level quality control.
Betahistine CoA mostly includes findings from lab analyses of a specific batch. For each Betahistine 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.
Betahistine may be tested according to a variety of international standards, such as European Pharmacopoeia (Betahistine EP), Betahistine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Betahistine USP).
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