Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
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
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
Sigma-Aldrich empowers scientific discovery with top-quality solutions to accelerate research, innovation, and better health worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35931
Submission : 2021-07-27
Status :
Type : II
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
EUROAPI
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Brand Name : Citric Acid Monohydrate
Application : Thickeners and Stabilizers
Excipient Details : Used as a pH regulator and preservative in many Biological formulations and cell culture media. Also it can be used as a chelating agent.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised packaging (from grs to kilograms)
Ingredient(s) : Citric Acid Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Thickeners and Stabilizers
Excipient Details : Used as carbon source in cell cultures in upstream, cryoprotectant and stabilizer in lyophilized formulations.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised packaging (from grs to kilograms)
Ingredient(s) : Saccharose Excipient
High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.
Dosage Form : Injectable / Parenteral
Grade : Biopharma Grade
Application : Parenteral
Excipient Details : Used as an osmolarity agent in culture media, tonicity adjuster in ophthalmics and parenterals solutions.
Pharmacopoeia Ref : On Request
Technical Specs : Low bacteria endotoxins, low bioburden (TAMC/TYMC). Customised packaging (from grs to kilograms)
Ingredient(s) : Sodium Chloride Excipient
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]CD Formulation
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]Kerry
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]Nitika Pharmaceutical Specialities
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 Chemical
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]Parenteral
Lubricants & Glidants
Fillers, Diluents & Binders
Thickeners and Stabilizers
Taste Masking
Coating Systems & Additives
Topical
Granulation
Direct Compression
Chewable & Orodispersible Aids
Emulsifying Agents
Controlled & Modified Release
Film Formers & Plasticizers
Co-Processed Excipients
ANALYTICAL
Analytical Methods
ABOUT THIS PAGE
53
PharmaCompass offers a list of Sodium Pyruvate 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 Sodium Pyruvate manufacturer or Sodium Pyruvate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Pyruvate manufacturer or Sodium Pyruvate supplier.
PharmaCompass also assists you with knowing the Sodium Pyruvate API Price utilized in the formulation of products. Sodium Pyruvate API Price is not always fixed or binding as the Sodium Pyruvate Price is obtained through a variety of data sources. The Sodium Pyruvate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Pyruvate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Pyruvate, including repackagers and relabelers. The FDA regulates Sodium Pyruvate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Pyruvate 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 Sodium Pyruvate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Pyruvate supplier is an individual or a company that provides Sodium Pyruvate active pharmaceutical ingredient (API) or Sodium Pyruvate finished formulations upon request. The Sodium Pyruvate suppliers may include Sodium Pyruvate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Pyruvate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Pyruvate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Pyruvate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Pyruvate DMFs exist exist since differing nations have different regulations, such as Sodium Pyruvate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Pyruvate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Pyruvate USDMF includes data on Sodium Pyruvate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Pyruvate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Pyruvate suppliers with USDMF on PharmaCompass.
Sodium Pyruvate 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 Sodium Pyruvate 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 Sodium Pyruvate GMP manufacturer or Sodium Pyruvate GMP API supplier for your needs.
A Sodium Pyruvate CoA (Certificate of Analysis) is a formal document that attests to Sodium Pyruvate's compliance with Sodium Pyruvate specifications and serves as a tool for batch-level quality control.
Sodium Pyruvate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Pyruvate 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.
Sodium Pyruvate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Pyruvate EP), Sodium Pyruvate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Pyruvate USP).
