Synopsis
0
USDMF
0
JDMF
0
VMF
0
FDA Orange Book
0
Canada
0
Australia
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
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 
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Evonik
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]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]Kewpie Corporation
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]Pfanstiehl
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]Corel Pharma Chem
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]Huzhou Sunflower Pharmaceutical
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]Lubrizol Life Science Health
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]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]Shijiazhuang Huaxu Pharmaceutical
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]Vasa Pharmachem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Zhejiang Huakang Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Direct Compression
Thickeners and Stabilizers
Topical
Taste Masking
Parenteral
Film Formers & Plasticizers
Co-Processed Excipients
Granulation
Chewable & Orodispersible Aids
Coating Systems & Additives
Lubricants & Glidants
Emulsifying Agents
Controlled & Modified Release
Disintegrants & Superdisintegrants
Solubilizers
API Stability Enhancers
Surfactant & Foaming Agents
Soft Gelatin
Rheology Modifiers
Digital Content
NEWS #PharmaBuzz
Market Place
ABOUT THIS PAGE
A Magnesium Sulfate Heptahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Sulfate Heptahydrate, including repackagers and relabelers. The FDA regulates Magnesium Sulfate Heptahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magnesium Sulfate Heptahydrate supplier is an individual or a company that provides Magnesium Sulfate Heptahydrate active pharmaceutical ingredient (API) or Magnesium Sulfate Heptahydrate finished formulations upon request. The Magnesium Sulfate Heptahydrate suppliers may include Magnesium Sulfate Heptahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Magnesium Sulfate Heptahydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Magnesium Sulfate Heptahydrate Drug Master File in Korea (Magnesium Sulfate Heptahydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Magnesium Sulfate Heptahydrate. The MFDS reviews the Magnesium Sulfate Heptahydrate KDMF as part of the drug registration process and uses the information provided in the Magnesium Sulfate Heptahydrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Magnesium Sulfate Heptahydrate suppliers with KDMF on PharmaCompass.
A Magnesium Sulfate Heptahydrate CEP of the European Pharmacopoeia monograph is often referred to as a Magnesium Sulfate Heptahydrate Certificate of Suitability (COS). The purpose of a Magnesium Sulfate Heptahydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Magnesium Sulfate Heptahydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Magnesium Sulfate Heptahydrate to their clients by showing that a Magnesium Sulfate Heptahydrate CEP has been issued for it. The manufacturer submits a Magnesium Sulfate Heptahydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Magnesium Sulfate Heptahydrate CEP holder for the record. Additionally, the data presented in the Magnesium Sulfate Heptahydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Magnesium Sulfate Heptahydrate DMF.
A Magnesium Sulfate Heptahydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate suppliers with CEP (COS) on PharmaCompass.
A Magnesium Sulfate Heptahydrate written confirmation (Magnesium Sulfate Heptahydrate WC) is an official document issued by a regulatory agency to a Magnesium Sulfate Heptahydrate manufacturer, verifying that the manufacturing facility of a Magnesium Sulfate Heptahydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Magnesium Sulfate Heptahydrate APIs or Magnesium Sulfate Heptahydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Magnesium Sulfate Heptahydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Magnesium Sulfate Heptahydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Magnesium Sulfate Heptahydrate suppliers with NDC on PharmaCompass.
Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate 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 Magnesium Sulfate Heptahydrate GMP manufacturer or Magnesium Sulfate Heptahydrate GMP API supplier for your needs.
A Magnesium Sulfate Heptahydrate CoA (Certificate of Analysis) is a formal document that attests to Magnesium Sulfate Heptahydrate's compliance with Magnesium Sulfate Heptahydrate specifications and serves as a tool for batch-level quality control.
Magnesium Sulfate Heptahydrate CoA mostly includes findings from lab analyses of a specific batch. For each Magnesium Sulfate Heptahydrate 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.
Magnesium Sulfate Heptahydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Magnesium Sulfate Heptahydrate EP), Magnesium Sulfate Heptahydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magnesium Sulfate Heptahydrate USP).
LOOKING FOR A SUPPLIER?
