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API SUPPLIERS
DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
HRV Pharma - Market Expansion Leader in Pharmaceuticals.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
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DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
Tenofovir Alafenamide Fumarate
About the Company : DKSH, founded with the goal of improving people's lives, assists businesses with market expansion and business growth in both existing and emerging markets. It has been fostering g...
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Tenofovir Alafenamide Fumarate
About the Company : Gonane Pharma, is a contract pharmaceutical company located in Gujarat, India, specializing in the manufacturing and marketing of Corticosteroids, Hormones, Antivirals, and Oncolog...
HRV Pharma - Market Expansion Leader in Pharmaceuticals.
Tenofovir Alafenamide Fumarate
About the Company : HRV Pharma is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
Tenofovir Alafenamide Fumarate
About the Company : Headquartered in Fengxian District, Shanghai Minbiotech Co., Ltd. is a company specializing in the R&D and production of advanced pharmaceutical intermediates and biological API...
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DOSAGE - TABLET;ORAL - 150MG;150MG;200MG;EQ 1...DOSAGE - TABLET;ORAL - 150MG;150MG;200MG;EQ 10MG BASE
USFDA APPLICATION NUMBER - 207561
DOSAGE - TABLET;ORAL - 120MG;EQ 15MG BASE
USFDA APPLICATION NUMBER - 208215
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USFDA APPLICATION NUMBER - 208215
DOSAGE - TABLET;ORAL - 200MG;EQ 25MG BASE;EQ ...DOSAGE - TABLET;ORAL - 200MG;EQ 25MG BASE;EQ 25MG BASE
USFDA APPLICATION NUMBER - 208351
DOSAGE - TABLET;ORAL - EQ 30MG BASE;120MG;EQ ...DOSAGE - TABLET;ORAL - EQ 30MG BASE;120MG;EQ 15MG BASE
USFDA APPLICATION NUMBER - 210251
DOSAGE - TABLET;ORAL - EQ 50MG BASE;200MG;EQ ...DOSAGE - TABLET;ORAL - EQ 50MG BASE;200MG;EQ 25MG BASE
USFDA APPLICATION NUMBER - 210251
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ABOUT THIS PAGE
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PharmaCompass offers a list of Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate manufacturer or Tenofovir Alafenamide Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tenofovir Alafenamide Fumarate manufacturer or Tenofovir Alafenamide Fumarate supplier.
PharmaCompass also assists you with knowing the Tenofovir Alafenamide Fumarate API Price utilized in the formulation of products. Tenofovir Alafenamide Fumarate API Price is not always fixed or binding as the Tenofovir Alafenamide Fumarate Price is obtained through a variety of data sources. The Tenofovir Alafenamide Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tenofovir Alafenamide Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenofovir Alafenamide Fumarate, including repackagers and relabelers. The FDA regulates Tenofovir Alafenamide Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenofovir Alafenamide Fumarate supplier is an individual or a company that provides Tenofovir Alafenamide Fumarate active pharmaceutical ingredient (API) or Tenofovir Alafenamide Fumarate finished formulations upon request. The Tenofovir Alafenamide Fumarate suppliers may include Tenofovir Alafenamide Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tenofovir Alafenamide Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenofovir Alafenamide Fumarate DMF (Drug Master File) is a document detailing the whole manufacturing process of Tenofovir Alafenamide Fumarate active pharmaceutical ingredient (API) in detail. Different forms of Tenofovir Alafenamide Fumarate DMFs exist exist since differing nations have different regulations, such as Tenofovir Alafenamide Fumarate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tenofovir Alafenamide Fumarate DMF submitted to regulatory agencies in the US is known as a USDMF. Tenofovir Alafenamide Fumarate USDMF includes data on Tenofovir Alafenamide Fumarate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tenofovir Alafenamide Fumarate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate Drug Master File in Korea (Tenofovir Alafenamide Fumarate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tenofovir Alafenamide Fumarate. The MFDS reviews the Tenofovir Alafenamide Fumarate KDMF as part of the drug registration process and uses the information provided in the Tenofovir Alafenamide Fumarate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tenofovir Alafenamide Fumarate suppliers with KDMF on PharmaCompass.
A Tenofovir Alafenamide Fumarate written confirmation (Tenofovir Alafenamide Fumarate WC) is an official document issued by a regulatory agency to a Tenofovir Alafenamide Fumarate manufacturer, verifying that the manufacturing facility of a Tenofovir Alafenamide Fumarate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tenofovir Alafenamide Fumarate APIs or Tenofovir Alafenamide Fumarate finished pharmaceutical products to another nation, regulatory agencies frequently require a Tenofovir Alafenamide Fumarate WC (written confirmation) as part of the regulatory process.
click here to find a list of Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tenofovir Alafenamide Fumarate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tenofovir Alafenamide Fumarate suppliers with NDC on PharmaCompass.
Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate 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 Tenofovir Alafenamide Fumarate GMP manufacturer or Tenofovir Alafenamide Fumarate GMP API supplier for your needs.
A Tenofovir Alafenamide Fumarate CoA (Certificate of Analysis) is a formal document that attests to Tenofovir Alafenamide Fumarate's compliance with Tenofovir Alafenamide Fumarate specifications and serves as a tool for batch-level quality control.
Tenofovir Alafenamide Fumarate CoA mostly includes findings from lab analyses of a specific batch. For each Tenofovir Alafenamide Fumarate 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.
Tenofovir Alafenamide Fumarate may be tested according to a variety of international standards, such as European Pharmacopoeia (Tenofovir Alafenamide Fumarate EP), Tenofovir Alafenamide Fumarate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tenofovir Alafenamide Fumarate USP).
