Synopsis
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CEP/COS
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JDMF
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1. Anhydrous Sodium Citrate
2. Citra Ph
3. Monosodium Citrate
4. Sodium Citrate
5. Sodium Citrate Dihydrate
6. Sodium Citrate Monobasic
7. Sodium Citrate, Anhydrous
8. Trisodium Citrate Dihydrate
1. Citrofluyl
2. Monosodium Dihydrogen Citrate
3. Citric Acid, Monosodium Salt
4. Citric Acid Monosodium Salt
5. Sodium Citrate Monobasic
6. 68538up9se
7. Sodium Dihydrogen Citrate Anhydrous
8. Einecs 242-734-6
9. Unii-68538up9se
10. 1,2,3-propanetricarboxylic Acid, 2-hydroxy-, Sodium Salt (1:1)
11. Ec 242-734-6
12. E82980
| Molecular Weight | 214.10 g/mol |
|---|---|
| Molecular Formula | C6H7NaO7 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 214.00894684 g/mol |
| Monoisotopic Mass | 214.00894684 g/mol |
| Topological Polar Surface Area | 135 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 233 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Anticoagulants
Agents that prevent BLOOD CLOTTING. (See all compounds classified as Anticoagulants.)
Buffers
A chemical system that functions to control the levels of specific ions in solution. When the level of hydrogen ion in solution is controlled the system is called a pH buffer. (See all compounds classified as Buffers.)
Food Preservatives
Substances capable of inhibiting, retarding or arresting the process of fermentation, acidification or other deterioration of foods. (See all compounds classified as Food Preservatives.)
API SUPPLIERS
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39459
Submission : 2024-02-06
Status : Active
Type : IV
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A Sodium Dihydrogen Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Dihydrogen Citrate, including repackagers and relabelers. The FDA regulates Sodium Dihydrogen Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Dihydrogen 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 Sodium Dihydrogen Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Dihydrogen Citrate supplier is an individual or a company that provides Sodium Dihydrogen Citrate active pharmaceutical ingredient (API) or Sodium Dihydrogen Citrate finished formulations upon request. The Sodium Dihydrogen Citrate suppliers may include Sodium Dihydrogen Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Dihydrogen Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Dihydrogen Citrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Dihydrogen Citrate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Dihydrogen Citrate DMFs exist exist since differing nations have different regulations, such as Sodium Dihydrogen Citrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Dihydrogen Citrate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Dihydrogen Citrate USDMF includes data on Sodium Dihydrogen Citrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Dihydrogen Citrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Dihydrogen Citrate suppliers with USDMF on PharmaCompass.
Sodium Dihydrogen 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 Sodium Dihydrogen Citrate 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 Dihydrogen Citrate GMP manufacturer or Sodium Dihydrogen Citrate GMP API supplier for your needs.
A Sodium Dihydrogen Citrate CoA (Certificate of Analysis) is a formal document that attests to Sodium Dihydrogen Citrate's compliance with Sodium Dihydrogen Citrate specifications and serves as a tool for batch-level quality control.
Sodium Dihydrogen Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Dihydrogen 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.
Sodium Dihydrogen Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Dihydrogen Citrate EP), Sodium Dihydrogen Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Dihydrogen Citrate USP).
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