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