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KDMF
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FDA Orange Book
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
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USDMF
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API Imports and Exports
Drugs in Development
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EUROAPI
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REF. STANDARDS & IMPURITIES
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ABOUT THIS PAGE
32
PharmaCompass offers a list of Sennoside A & B 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 Sennoside A & B manufacturer or Sennoside A & B supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sennoside A & B manufacturer or Sennoside A & B supplier.
PharmaCompass also assists you with knowing the Sennoside A & B API Price utilized in the formulation of products. Sennoside A & B API Price is not always fixed or binding as the Sennoside A & B Price is obtained through a variety of data sources. The Sennoside A & B Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Senokot manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Senokot, including repackagers and relabelers. The FDA regulates Senokot manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Senokot 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 Senokot manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Senokot supplier is an individual or a company that provides Senokot active pharmaceutical ingredient (API) or Senokot finished formulations upon request. The Senokot suppliers may include Senokot API manufacturers, exporters, distributors and traders.
click here to find a list of Senokot suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Senokot DMF (Drug Master File) is a document detailing the whole manufacturing process of Senokot active pharmaceutical ingredient (API) in detail. Different forms of Senokot DMFs exist exist since differing nations have different regulations, such as Senokot USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Senokot DMF submitted to regulatory agencies in the US is known as a USDMF. Senokot USDMF includes data on Senokot's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Senokot USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Senokot 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 Senokot Drug Master File in Japan (Senokot JDMF) empowers Senokot 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 Senokot JDMF during the approval evaluation for pharmaceutical products. At the time of Senokot 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 Senokot suppliers with JDMF on PharmaCompass.
A Senokot written confirmation (Senokot WC) is an official document issued by a regulatory agency to a Senokot manufacturer, verifying that the manufacturing facility of a Senokot active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Senokot APIs or Senokot finished pharmaceutical products to another nation, regulatory agencies frequently require a Senokot WC (written confirmation) as part of the regulatory process.
click here to find a list of Senokot 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 Senokot as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Senokot 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 Senokot 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 Senokot and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Senokot NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Senokot suppliers with NDC on PharmaCompass.
Senokot 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 Senokot 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 Senokot GMP manufacturer or Senokot GMP API supplier for your needs.
A Senokot CoA (Certificate of Analysis) is a formal document that attests to Senokot's compliance with Senokot specifications and serves as a tool for batch-level quality control.
Senokot CoA mostly includes findings from lab analyses of a specific batch. For each Senokot 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.
Senokot may be tested according to a variety of international standards, such as European Pharmacopoeia (Senokot EP), Senokot JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Senokot USP).
