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