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