Synopsis
0
JDMF
0
VMF
0
Australia
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Boai NKY Pharmaceuticals Ltd
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
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Aeon Procare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Alcedo Pharmachem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DFE Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ideal Cures Pvt Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ingredion Pharma Solutions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kerry
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Bold Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Novo Excipients
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharmatrans-Sanaq
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pluviaendo
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Prachin Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Roquette
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seppic
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Welltone Material Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ulanqab Kema New Material
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Direct Compression
Disintegrants & Superdisintegrants
Thickeners and Stabilizers
Co-Processed Excipients
Solubilizers
Granulation
Lubricants & Glidants
Chewable & Orodispersible Aids
Emulsifying Agents
Parenteral
Controlled & Modified Release
Film Formers & Plasticizers
Coating Systems & Additives
Taste Masking
Topical
API Stability Enhancers
Rheology Modifiers
Surfactant & Foaming Agents
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Mefloquine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mefloquine, including repackagers and relabelers. The FDA regulates Mefloquine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mefloquine 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 Mefloquine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mefloquine supplier is an individual or a company that provides Mefloquine active pharmaceutical ingredient (API) or Mefloquine finished formulations upon request. The Mefloquine suppliers may include Mefloquine API manufacturers, exporters, distributors and traders.
click here to find a list of Mefloquine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mefloquine DMF (Drug Master File) is a document detailing the whole manufacturing process of Mefloquine active pharmaceutical ingredient (API) in detail. Different forms of Mefloquine DMFs exist exist since differing nations have different regulations, such as Mefloquine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mefloquine DMF submitted to regulatory agencies in the US is known as a USDMF. Mefloquine USDMF includes data on Mefloquine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mefloquine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mefloquine 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 Mefloquine Drug Master File in Korea (Mefloquine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Mefloquine. The MFDS reviews the Mefloquine KDMF as part of the drug registration process and uses the information provided in the Mefloquine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Mefloquine 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 Mefloquine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Mefloquine suppliers with KDMF on PharmaCompass.
A Mefloquine CEP of the European Pharmacopoeia monograph is often referred to as a Mefloquine Certificate of Suitability (COS). The purpose of a Mefloquine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mefloquine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mefloquine to their clients by showing that a Mefloquine CEP has been issued for it. The manufacturer submits a Mefloquine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mefloquine CEP holder for the record. Additionally, the data presented in the Mefloquine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mefloquine DMF.
A Mefloquine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mefloquine 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 Mefloquine suppliers with CEP (COS) on PharmaCompass.
A Mefloquine written confirmation (Mefloquine WC) is an official document issued by a regulatory agency to a Mefloquine manufacturer, verifying that the manufacturing facility of a Mefloquine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Mefloquine APIs or Mefloquine finished pharmaceutical products to another nation, regulatory agencies frequently require a Mefloquine WC (written confirmation) as part of the regulatory process.
click here to find a list of Mefloquine 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 Mefloquine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mefloquine 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 Mefloquine 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 Mefloquine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mefloquine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mefloquine suppliers with NDC on PharmaCompass.
Mefloquine 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 Mefloquine 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 Mefloquine GMP manufacturer or Mefloquine GMP API supplier for your needs.
A Mefloquine CoA (Certificate of Analysis) is a formal document that attests to Mefloquine's compliance with Mefloquine specifications and serves as a tool for batch-level quality control.
Mefloquine CoA mostly includes findings from lab analyses of a specific batch. For each Mefloquine 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.
Mefloquine may be tested according to a variety of international standards, such as European Pharmacopoeia (Mefloquine EP), Mefloquine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mefloquine USP).
LOOKING FOR A SUPPLIER?
