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API SUPPLIERS
Jai Radhe Sales is your partner for all your sourcing needs.
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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USDMF
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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : OTC
Registration Country : Canada
Brand Name : GOLD BOND ANTI-ITCH LOTION
Dosage Form : LOTION
Dosage Strength : 5%/W/W
Packaging : 155ML
Approval Date :
Application Number : 2318482
Regulatory Info : OTC
Registration Country : Canada
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Dimethicone 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 Dimethicone manufacturer or Dimethicone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimethicone manufacturer or Dimethicone supplier.
PharmaCompass also assists you with knowing the Dimethicone API Price utilized in the formulation of products. Dimethicone API Price is not always fixed or binding as the Dimethicone Price is obtained through a variety of data sources. The Dimethicone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DIMETHYLPOLYSILOXANE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIMETHYLPOLYSILOXANE, including repackagers and relabelers. The FDA regulates DIMETHYLPOLYSILOXANE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DIMETHYLPOLYSILOXANE supplier is an individual or a company that provides DIMETHYLPOLYSILOXANE active pharmaceutical ingredient (API) or DIMETHYLPOLYSILOXANE finished formulations upon request. The DIMETHYLPOLYSILOXANE suppliers may include DIMETHYLPOLYSILOXANE API manufacturers, exporters, distributors and traders.
click here to find a list of DIMETHYLPOLYSILOXANE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DIMETHYLPOLYSILOXANE DMF (Drug Master File) is a document detailing the whole manufacturing process of DIMETHYLPOLYSILOXANE active pharmaceutical ingredient (API) in detail. Different forms of DIMETHYLPOLYSILOXANE DMFs exist exist since differing nations have different regulations, such as DIMETHYLPOLYSILOXANE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DIMETHYLPOLYSILOXANE DMF submitted to regulatory agencies in the US is known as a USDMF. DIMETHYLPOLYSILOXANE USDMF includes data on DIMETHYLPOLYSILOXANE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DIMETHYLPOLYSILOXANE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE Drug Master File in Japan (DIMETHYLPOLYSILOXANE JDMF) empowers DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE JDMF during the approval evaluation for pharmaceutical products. At the time of DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE suppliers with JDMF on PharmaCompass.
A DIMETHYLPOLYSILOXANE CEP of the European Pharmacopoeia monograph is often referred to as a DIMETHYLPOLYSILOXANE Certificate of Suitability (COS). The purpose of a DIMETHYLPOLYSILOXANE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DIMETHYLPOLYSILOXANE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DIMETHYLPOLYSILOXANE to their clients by showing that a DIMETHYLPOLYSILOXANE CEP has been issued for it. The manufacturer submits a DIMETHYLPOLYSILOXANE CEP (COS) as part of the market authorization procedure, and it takes on the role of a DIMETHYLPOLYSILOXANE CEP holder for the record. Additionally, the data presented in the DIMETHYLPOLYSILOXANE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DIMETHYLPOLYSILOXANE DMF.
A DIMETHYLPOLYSILOXANE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE suppliers with CEP (COS) on PharmaCompass.
A DIMETHYLPOLYSILOXANE written confirmation (DIMETHYLPOLYSILOXANE WC) is an official document issued by a regulatory agency to a DIMETHYLPOLYSILOXANE manufacturer, verifying that the manufacturing facility of a DIMETHYLPOLYSILOXANE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DIMETHYLPOLYSILOXANE APIs or DIMETHYLPOLYSILOXANE finished pharmaceutical products to another nation, regulatory agencies frequently require a DIMETHYLPOLYSILOXANE WC (written confirmation) as part of the regulatory process.
click here to find a list of DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DIMETHYLPOLYSILOXANE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DIMETHYLPOLYSILOXANE suppliers with NDC on PharmaCompass.
DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE 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 DIMETHYLPOLYSILOXANE GMP manufacturer or DIMETHYLPOLYSILOXANE GMP API supplier for your needs.
A DIMETHYLPOLYSILOXANE CoA (Certificate of Analysis) is a formal document that attests to DIMETHYLPOLYSILOXANE's compliance with DIMETHYLPOLYSILOXANE specifications and serves as a tool for batch-level quality control.
DIMETHYLPOLYSILOXANE CoA mostly includes findings from lab analyses of a specific batch. For each DIMETHYLPOLYSILOXANE 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.
DIMETHYLPOLYSILOXANE may be tested according to a variety of international standards, such as European Pharmacopoeia (DIMETHYLPOLYSILOXANE EP), DIMETHYLPOLYSILOXANE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DIMETHYLPOLYSILOXANE USP).
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