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KDMF
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VMF
DRUG PRODUCT COMPOSITIONS
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US Patents
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Health Canada Patents
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Jai Radhe Sales is your partner for all your sourcing needs.
Boai NKY Pharmaceuticals Ltd. is one of the largest global PVP suppliers.
Chynops Pharma is an ideal sourcing partner for high-quality APIs, advanced intermediates, speciality chemicals & excipients.
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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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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EUROAPI
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Solubilizers
Thickeners and Stabilizers
Parenteral
Film Formers & Plasticizers
Fillers, Diluents & Binders
Coating Systems & Additives
Direct Compression
Lubricants & Glidants
Co-Processed Excipients
Taste Masking
Surfactant & Foaming Agents
Rheology Modifiers
Controlled & Modified Release
Emulsifying Agents
Granulation
Chewable & Orodispersible Aids
API Stability Enhancers
Disintegrants & Superdisintegrants
Digital Content
DATA COMPILATION #PharmaFlow
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 Povidone Iodine 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 Povidone Iodine manufacturer or Povidone Iodine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Povidone Iodine manufacturer or Povidone Iodine supplier.
PharmaCompass also assists you with knowing the Povidone Iodine API Price utilized in the formulation of products. Povidone Iodine API Price is not always fixed or binding as the Povidone Iodine Price is obtained through a variety of data sources. The Povidone Iodine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Betadines manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betadines, including repackagers and relabelers. The FDA regulates Betadines manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betadines 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 Betadines manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Betadines supplier is an individual or a company that provides Betadines active pharmaceutical ingredient (API) or Betadines finished formulations upon request. The Betadines suppliers may include Betadines API manufacturers, exporters, distributors and traders.
click here to find a list of Betadines suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Betadines DMF (Drug Master File) is a document detailing the whole manufacturing process of Betadines active pharmaceutical ingredient (API) in detail. Different forms of Betadines DMFs exist exist since differing nations have different regulations, such as Betadines USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Betadines DMF submitted to regulatory agencies in the US is known as a USDMF. Betadines USDMF includes data on Betadines's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Betadines USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Betadines 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 Betadines Drug Master File in Japan (Betadines JDMF) empowers Betadines 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 Betadines JDMF during the approval evaluation for pharmaceutical products. At the time of Betadines 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 Betadines suppliers with JDMF on PharmaCompass.
A Betadines CEP of the European Pharmacopoeia monograph is often referred to as a Betadines Certificate of Suitability (COS). The purpose of a Betadines CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Betadines EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Betadines to their clients by showing that a Betadines CEP has been issued for it. The manufacturer submits a Betadines CEP (COS) as part of the market authorization procedure, and it takes on the role of a Betadines CEP holder for the record. Additionally, the data presented in the Betadines CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Betadines DMF.
A Betadines CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Betadines 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 Betadines suppliers with CEP (COS) on PharmaCompass.
A Betadines written confirmation (Betadines WC) is an official document issued by a regulatory agency to a Betadines manufacturer, verifying that the manufacturing facility of a Betadines active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Betadines APIs or Betadines finished pharmaceutical products to another nation, regulatory agencies frequently require a Betadines WC (written confirmation) as part of the regulatory process.
click here to find a list of Betadines 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 Betadines as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Betadines 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 Betadines 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 Betadines and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Betadines NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Betadines suppliers with NDC on PharmaCompass.
Betadines 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 Betadines 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 Betadines GMP manufacturer or Betadines GMP API supplier for your needs.
A Betadines CoA (Certificate of Analysis) is a formal document that attests to Betadines's compliance with Betadines specifications and serves as a tool for batch-level quality control.
Betadines CoA mostly includes findings from lab analyses of a specific batch. For each Betadines 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.
Betadines may be tested according to a variety of international standards, such as European Pharmacopoeia (Betadines EP), Betadines JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Betadines USP).
