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VMF
DRUG PRODUCT COMPOSITIONS0
Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
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USDMF
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API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
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DOSAGE - INJECTABLE;INTRAVENOUS - 100MG/20ML ...DOSAGE - INJECTABLE;INTRAVENOUS - 100MG/20ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21759
DOSAGE - INJECTABLE;INTRAVENOUS - 200MG/40ML ...DOSAGE - INJECTABLE;INTRAVENOUS - 200MG/40ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21759
DOSAGE - INJECTABLE;INTRAVENOUS - 50MG/10ML (...DOSAGE - INJECTABLE;INTRAVENOUS - 50MG/10ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21759
DOSAGE - INJECTABLE;INTRAVENOUS - 100MG/20ML ...DOSAGE - INJECTABLE;INTRAVENOUS - 100MG/20ML (5MG/ML)
USFDA APPLICATION NUMBER - 22160
DOSAGE - INJECTABLE;INTRAVENOUS - 50MG/10ML (...DOSAGE - INJECTABLE;INTRAVENOUS - 50MG/10ML (5MG/ML)
USFDA APPLICATION NUMBER - 22160
Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Granulation
Direct Compression
Solubilizers
Co-Processed Excipients
Parenteral
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Oxaliplatin 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 Oxaliplatin manufacturer or Oxaliplatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxaliplatin manufacturer or Oxaliplatin supplier.
PharmaCompass also assists you with knowing the Oxaliplatin API Price utilized in the formulation of products. Oxaliplatin API Price is not always fixed or binding as the Oxaliplatin Price is obtained through a variety of data sources. The Oxaliplatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ACT 078 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACT 078, including repackagers and relabelers. The FDA regulates ACT 078 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACT 078 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 ACT 078 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ACT 078 supplier is an individual or a company that provides ACT 078 active pharmaceutical ingredient (API) or ACT 078 finished formulations upon request. The ACT 078 suppliers may include ACT 078 API manufacturers, exporters, distributors and traders.
click here to find a list of ACT 078 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ACT 078 DMF (Drug Master File) is a document detailing the whole manufacturing process of ACT 078 active pharmaceutical ingredient (API) in detail. Different forms of ACT 078 DMFs exist exist since differing nations have different regulations, such as ACT 078 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ACT 078 DMF submitted to regulatory agencies in the US is known as a USDMF. ACT 078 USDMF includes data on ACT 078's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ACT 078 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ACT 078 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 ACT 078 Drug Master File in Japan (ACT 078 JDMF) empowers ACT 078 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 ACT 078 JDMF during the approval evaluation for pharmaceutical products. At the time of ACT 078 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 ACT 078 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 ACT 078 Drug Master File in Korea (ACT 078 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ACT 078. The MFDS reviews the ACT 078 KDMF as part of the drug registration process and uses the information provided in the ACT 078 KDMF to evaluate the safety and efficacy of the drug.
After submitting a ACT 078 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 ACT 078 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of ACT 078 suppliers with KDMF on PharmaCompass.
A ACT 078 CEP of the European Pharmacopoeia monograph is often referred to as a ACT 078 Certificate of Suitability (COS). The purpose of a ACT 078 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ACT 078 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ACT 078 to their clients by showing that a ACT 078 CEP has been issued for it. The manufacturer submits a ACT 078 CEP (COS) as part of the market authorization procedure, and it takes on the role of a ACT 078 CEP holder for the record. Additionally, the data presented in the ACT 078 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ACT 078 DMF.
A ACT 078 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ACT 078 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 ACT 078 suppliers with CEP (COS) on PharmaCompass.
A ACT 078 written confirmation (ACT 078 WC) is an official document issued by a regulatory agency to a ACT 078 manufacturer, verifying that the manufacturing facility of a ACT 078 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ACT 078 APIs or ACT 078 finished pharmaceutical products to another nation, regulatory agencies frequently require a ACT 078 WC (written confirmation) as part of the regulatory process.
click here to find a list of ACT 078 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 ACT 078 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ACT 078 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 ACT 078 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 ACT 078 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ACT 078 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ACT 078 suppliers with NDC on PharmaCompass.
ACT 078 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 ACT 078 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 ACT 078 GMP manufacturer or ACT 078 GMP API supplier for your needs.
A ACT 078 CoA (Certificate of Analysis) is a formal document that attests to ACT 078's compliance with ACT 078 specifications and serves as a tool for batch-level quality control.
ACT 078 CoA mostly includes findings from lab analyses of a specific batch. For each ACT 078 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.
ACT 078 may be tested according to a variety of international standards, such as European Pharmacopoeia (ACT 078 EP), ACT 078 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ACT 078 USP).
