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1. 2 Amino 2 Deoxyglucose
2. 2-amino-2-deoxyglucose
3. Dona
4. Dona S
5. Glucosamine
6. Hespercorbin
7. Sulfate, Glucosamine
8. Xicil
1. D-glucosamine Sulfate
2. 29031-19-4
3. (2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanal Sulfate
4. 33508-19-9
5. Glucosamine Sulphate
6. Dona
7. 2-amino-2-deoxy-d-glucose Sulfate (salt)
8. Gevolox
9. Arthro
10. Glucosaminsulfat
11. Sulfato De Glucosamina
12. Mfcd00135940
13. Einecs 249-379-6
14. Glucosamine Sulfate 2kcl
15. D-glucosamine Sulfate Salt
16. D-glucose, 2-amino-2-deoxy-, Sulfate (salt)
17. Glucosamine Sulfate Na Salt
18. Schembl22031
19. Glucosamine Sulfate Dc 95%
20. Dtxsid30944241
21. Hy-n0487
22. S3850
23. Ccg-267216
24. As-15566
25. Cs-0009005
26. Sulfuric Acid--2-amino-2-deoxyhexose (1/1)
27. A875270
28. W-107012
29. (2s,3s,5s)-3-amino-6-(hydroxymethyl)tetrahydropyran-2,4,5-triol
30. 216447-61-9
| Molecular Weight | 277.25 g/mol |
|---|---|
| Molecular Formula | C6H15NO9S |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 5 |
| Exact Mass | 277.04675223 g/mol |
| Monoisotopic Mass | 277.04675223 g/mol |
| Topological Polar Surface Area | 207 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 223 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
API SUPPLIERS
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14915
Submission : 2000-06-08
Status : Active
Type : II
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
NDC Package Code : 82051-003
Start Marketing Date : 2021-06-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
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Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
About the Company : Bioiberica is a global Life Science company with more than 45 years' experience in the production and development of molecules of high biological and therapeutic value for the phar...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
About the Company : Bioplus Life Sciences is a leading provider of contract research, development, distribution and manufacturing services for licensed and OTC (nutritional) pharmaceuticals. With a gl...
About the Company : Summit ingredient Co.,Ltd is a leading and rapidly growing company wh ich engages in the production, development, source and sale of botanical extracts . Summit located in Shaanxi ...
About the Company : SWATI SPENTOSE PVT. LTD.(SSPL), a pharmaceutical company based in Mumbai, India having 2 manufacturing sites: SSPL Unit 1 and SSPL Unit 2. Please find attached a brief presentation...
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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Drugs in Development
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Grade : Oral
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Pharmacopoeia Ref : NA
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Ingredient(s) : Microcrystalline Cellulose
SPI Pharma has been solving formulation challenges using superior functional materials.
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Pharmacopoeia Ref : NA
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Ingredient(s) : Starch
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Glucosamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucosamine, including repackagers and relabelers. The FDA regulates Glucosamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucosamine 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 Glucosamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucosamine supplier is an individual or a company that provides Glucosamine active pharmaceutical ingredient (API) or Glucosamine finished formulations upon request. The Glucosamine suppliers may include Glucosamine API manufacturers, exporters, distributors and traders.
click here to find a list of Glucosamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glucosamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Glucosamine active pharmaceutical ingredient (API) in detail. Different forms of Glucosamine DMFs exist exist since differing nations have different regulations, such as Glucosamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glucosamine DMF submitted to regulatory agencies in the US is known as a USDMF. Glucosamine USDMF includes data on Glucosamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glucosamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glucosamine suppliers with USDMF 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 Glucosamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glucosamine 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 Glucosamine 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 Glucosamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glucosamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glucosamine suppliers with NDC on PharmaCompass.
Glucosamine 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 Glucosamine 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 Glucosamine GMP manufacturer or Glucosamine GMP API supplier for your needs.
A Glucosamine CoA (Certificate of Analysis) is a formal document that attests to Glucosamine's compliance with Glucosamine specifications and serves as a tool for batch-level quality control.
Glucosamine CoA mostly includes findings from lab analyses of a specific batch. For each Glucosamine 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.
Glucosamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Glucosamine EP), Glucosamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glucosamine USP).
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