Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
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USDMF
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Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Pharm-Rx has earned an outstanding reputation since its establishment in 1991, serving as a reputable importer and distributor of active ingredients to the pharmaceutical, nutritio...
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Coating Systems & Additives
Disintegrants & Superdisintegrants
Solubilizers
Direct Compression
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Controlled & Modified Release
Granulation
Topical
Lubricants & Glidants
Co-Processed Excipients
Film Formers & Plasticizers
Chewable & Orodispersible Aids
Parenteral
Taste Masking
Emulsifying Agents
Rheology Modifiers
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Empty Capsules
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Surfactant & Foaming Agents
Coloring Agents
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
57
PharmaCompass offers a list of Magnesium Salicylate 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 Magnesium Salicylate manufacturer or Magnesium Salicylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Salicylate manufacturer or Magnesium Salicylate supplier.
PharmaCompass also assists you with knowing the Magnesium Salicylate API Price utilized in the formulation of products. Magnesium Salicylate API Price is not always fixed or binding as the Magnesium Salicylate Price is obtained through a variety of data sources. The Magnesium Salicylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Doan's manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doan's, including repackagers and relabelers. The FDA regulates Doan's manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doan's 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 Doan's manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doan's supplier is an individual or a company that provides Doan's active pharmaceutical ingredient (API) or Doan's finished formulations upon request. The Doan's suppliers may include Doan's API manufacturers, exporters, distributors and traders.
click here to find a list of Doan's suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doan's DMF (Drug Master File) is a document detailing the whole manufacturing process of Doan's active pharmaceutical ingredient (API) in detail. Different forms of Doan's DMFs exist exist since differing nations have different regulations, such as Doan's USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Doan's DMF submitted to regulatory agencies in the US is known as a USDMF. Doan's USDMF includes data on Doan's's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Doan's USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Doan's suppliers with USDMF 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 Doan's as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Doan's 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 Doan's 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 Doan's and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Doan's NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Doan's suppliers with NDC on PharmaCompass.
Doan's 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 Doan's 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 Doan's GMP manufacturer or Doan's GMP API supplier for your needs.
A Doan's CoA (Certificate of Analysis) is a formal document that attests to Doan's's compliance with Doan's specifications and serves as a tool for batch-level quality control.
Doan's CoA mostly includes findings from lab analyses of a specific batch. For each Doan's 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.
Doan's may be tested according to a variety of international standards, such as European Pharmacopoeia (Doan's EP), Doan's JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Doan's USP).
