Synopsis
0
KDMF
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
Australia
DRUG PRODUCT COMPOSITIONS0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Jai Radhe Sales is your partner for all your sourcing needs.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
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
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Rochem, established in 1994, is a global distributor of pharmaceutical, food, nutritional, and animal health ingredients, sourcing high-quality products from China. Headquartered i...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales, founded in 1999, is a global distributor specializing in high-quality pharmaceutical ingredients from India. It offers complete sourcing solutions, technical and r...
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
About the Company : Dr. Paul Lohmann® is a Germany based developer & manufacturer of high quality mineral salts with over 140 years of expertise. The company offers more than 400 salts in over 7,000 ...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 10ME...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 10MEQ
USFDA APPLICATION NUMBER - 19071
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 15ME...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 15MEQ
USFDA APPLICATION NUMBER - 19071
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 5MEQ
USFDA APPLICATION NUMBER - 19071
Related Excipient Companies
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]Pharm-RX Chemical
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]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dr. Paul Lohmann GmbH & Co. KGaA
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]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Bioplus Life Sciences
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CD Formulation
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Clariant
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Esteem Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Finar
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]Microlex e.U
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Neelkanth MineChem
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nitika Pharmaceutical Specialities
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nomisma Healthcare
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 Pharmachem
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]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]Silverline Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Valens Pharmachem
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]Topical
Film Formers & Plasticizers
Lubricants & Glidants
Thickeners and Stabilizers
Fillers, Diluents & Binders
Taste Masking
Coating Systems & Additives
Solubilizers
Parenteral
Controlled & Modified Release
Emulsifying Agents
API Stability Enhancers
Granulation
Direct Compression
Chewable & Orodispersible Aids
Co-Processed Excipients
Soft Gelatin
Surfactant & Foaming Agents
Rheology Modifiers
Digital Content
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
ABOUT THIS PAGE
73
PharmaCompass offers a list of Potassium Citrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Potassium Citrate manufacturer or Potassium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Citrate manufacturer or Potassium Citrate supplier.
A TRIPOTASSIUM CITRATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRIPOTASSIUM CITRATE, including repackagers and relabelers. The FDA regulates TRIPOTASSIUM CITRATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A TRIPOTASSIUM CITRATE supplier is an individual or a company that provides TRIPOTASSIUM CITRATE active pharmaceutical ingredient (API) or TRIPOTASSIUM CITRATE finished formulations upon request. The TRIPOTASSIUM CITRATE suppliers may include TRIPOTASSIUM CITRATE API manufacturers, exporters, distributors and traders.
click here to find a list of TRIPOTASSIUM CITRATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A TRIPOTASSIUM CITRATE DMF (Drug Master File) is a document detailing the whole manufacturing process of TRIPOTASSIUM CITRATE active pharmaceutical ingredient (API) in detail. Different forms of TRIPOTASSIUM CITRATE DMFs exist exist since differing nations have different regulations, such as TRIPOTASSIUM CITRATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A TRIPOTASSIUM CITRATE DMF submitted to regulatory agencies in the US is known as a USDMF. TRIPOTASSIUM CITRATE USDMF includes data on TRIPOTASSIUM CITRATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The TRIPOTASSIUM CITRATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE Drug Master File in Japan (TRIPOTASSIUM CITRATE JDMF) empowers TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE JDMF during the approval evaluation for pharmaceutical products. At the time of TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE suppliers with JDMF on PharmaCompass.
A TRIPOTASSIUM CITRATE CEP of the European Pharmacopoeia monograph is often referred to as a TRIPOTASSIUM CITRATE Certificate of Suitability (COS). The purpose of a TRIPOTASSIUM CITRATE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of TRIPOTASSIUM CITRATE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of TRIPOTASSIUM CITRATE to their clients by showing that a TRIPOTASSIUM CITRATE CEP has been issued for it. The manufacturer submits a TRIPOTASSIUM CITRATE CEP (COS) as part of the market authorization procedure, and it takes on the role of a TRIPOTASSIUM CITRATE CEP holder for the record. Additionally, the data presented in the TRIPOTASSIUM CITRATE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the TRIPOTASSIUM CITRATE DMF.
A TRIPOTASSIUM CITRATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE suppliers with CEP (COS) on PharmaCompass.
A TRIPOTASSIUM CITRATE written confirmation (TRIPOTASSIUM CITRATE WC) is an official document issued by a regulatory agency to a TRIPOTASSIUM CITRATE manufacturer, verifying that the manufacturing facility of a TRIPOTASSIUM CITRATE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting TRIPOTASSIUM CITRATE APIs or TRIPOTASSIUM CITRATE finished pharmaceutical products to another nation, regulatory agencies frequently require a TRIPOTASSIUM CITRATE WC (written confirmation) as part of the regulatory process.
click here to find a list of TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a TRIPOTASSIUM CITRATE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of TRIPOTASSIUM CITRATE suppliers with NDC on PharmaCompass.
TRIPOTASSIUM CITRATE 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 TRIPOTASSIUM CITRATE GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right TRIPOTASSIUM CITRATE GMP manufacturer or TRIPOTASSIUM CITRATE GMP API supplier for your needs.
A TRIPOTASSIUM CITRATE CoA (Certificate of Analysis) is a formal document that attests to TRIPOTASSIUM CITRATE's compliance with TRIPOTASSIUM CITRATE specifications and serves as a tool for batch-level quality control.
TRIPOTASSIUM CITRATE CoA mostly includes findings from lab analyses of a specific batch. For each TRIPOTASSIUM CITRATE 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.
TRIPOTASSIUM CITRATE may be tested according to a variety of international standards, such as European Pharmacopoeia (TRIPOTASSIUM CITRATE EP), TRIPOTASSIUM CITRATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TRIPOTASSIUM CITRATE USP).
