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