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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.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
SWATI - Transforming science into solutions with 60+ years of expertise, global accreditations, and pioneering biotech innovation.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14915
Submission : 2000-06-08
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
NDC Package Code : 82051-003
Start Marketing Date : 2021-06-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
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USDMF
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NDC Package Code : 82051-003
Start Marketing Date : 2021-06-28
End Marketing Date : 2026-12-31
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 over 45 years of experience developing & producing high‑value biological molecules for the pharmaceutical and nutraceutical indus...
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...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
SWATI - Transforming science into solutions with 60+ years of expertise, global accreditations, and pioneering biotech innovation.
About the Company : Swati Spentose Pvt. Ltd. (SSPL), part of the 60-year-old V Group, is a globally trusted pharmaceutical manufacturer supplying to 70+ countries. We specialize in high-quality APIs a...
About the Company : Anwita Drugs is a technocrat-driven pharmaceutical company with over 28 years of expertise in designing and developing solid oral dosage forms (OSD), nutraceuticals, and dietary su...
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 : Yangzhou Pharmaceutical Co., Ltd is one of the middle-scale state-owned comprehensive enterprises. It has fixed assets of RMB 22 million and covers land of area of 120 000m2. It em...
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Drugs in Development
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Towa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.
Regulatory Info : Suspended
Registration Country : Spain
Brand Name : Glucosamina Pensa
Dosage Form : Powder For Oral Solution
Dosage Strength : 1500MG
Packaging :
Approval Date : 25-10-2006
Application Number : 68106
Regulatory Info : Suspended
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Glucosamine Cinfa
Dosage Form : Powder For Oral Solution
Dosage Strength : 1500MG
Packaging :
Approval Date : 25-10-2006
Application Number : 68105
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Minedon
Dosage Form : Powder For Oral Solution
Dosage Strength : 1.5G
Packaging :
Approval Date : 2017-07-27
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info :
Registration Country : Moldova
Brand Name : Chondromed Plus
Dosage Form : Powder For Oral Solution
Dosage Strength : 600 mg; 750 mg
Packaging :
Approval Date : 29-11-2021
Application Number :
Regulatory Info :
Registration Country : Moldova
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Glucosamine Mabo
Dosage Form : Powder For Oral Solution
Dosage Strength : 1500MG
Packaging :
Approval Date : 20-06-2007
Application Number : 69005
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Glucosamine Pharma Nord
Dosage Form : Capsule
Dosage Strength : 400mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : SACHET
Dosage Strength : 1500MG
Packaging : 20 Sachets
Approval Date :
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Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info :
Registration Country : Italy
Brand Name : Dona
Dosage Form :
Dosage Strength : 6 Vials At + 6 Vials B 400 Mg
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Regulatory Info :
Registration Country : Italy
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Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Dolenio
Dosage Form : Film Coated Tablet
Dosage Strength : 1178MG
Packaging :
Approval Date : 2011-09-30
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Dolenio
Dosage Form : Film-Coated Tablet
Dosage Strength : 1178mg
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Regulatory Info : Prescription
Registration Country : Estonia
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Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Glucosamine; Chondroitin Sulfate Sodium
Brand Name : Glucosamine; Chondroit...
Dosage Form : Tablet
Dosage Strength : 500MG; 400MG
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Glucosamine; Chondroitin Sulfate Sodium
Dosage : Tablet
Dosage Strength : 500MG; 400MG
Brand Name : Glucosamine; Chondroit...
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Registration Country : India
Regulatory Info : Generic
Registration Country : Pakistan
Glucosamine Sulfate; Chondroitin Sulfate
Brand Name : Orthobio Extra
Dosage Form : FC TABLET
Dosage Strength : 500MG; 400MG
Packaging : as per requirement
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Pakistan
Packaging : as per requirement
Regulatory Info : Generic
Glucosamine Sulfate; Chondroitin Sulfate
Dosage : FC TABLET
Dosage Strength : 500MG; 400MG
Brand Name : Orthobio Extra
Approval Date :
Application Number :
Registration Country : Pakistan
Regulatory Info : Generic
Registration Country : Pakistan
Brand Name : Orthobio
Dosage Form : CAPSULE
Dosage Strength : 500MG
Packaging : as per requirement
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Pakistan
Packaging : as per requirement
Regulatory Info : Generic
Dosage : CAPSULE
Dosage Strength : 500MG
Brand Name : Orthobio
Approval Date :
Application Number :
Registration Country : Pakistan
Regulatory Info :
Registration Country : India
Diacerein; Dimethyl Sulfone; Glucosamine
Brand Name :
Dosage Form : Tablet
Dosage Strength : 50MG; 250MG; 75MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Diacerein; Dimethyl Sulfone; Glucosamine
Dosage : Tablet
Dosage Strength : 50MG; 250MG; 75MG
Brand Name :
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : India
Glucosamine Sulphate; Chondroitin Sulfate Sodium
Brand Name :
Dosage Form : Tablet; Tablet
Dosage Strength : 500MG; 400MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Glucosamine Sulphate; Chondroitin Sulfate Sodium
Dosage : Tablet; Tablet
Dosage Strength : 500MG; 400MG
Brand Name :
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : India
Glucosamine; Chondroitin Sulfate Sodium
Brand Name :
Dosage Form : Tablet
Dosage Strength : 500MG; 400MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Glucosamine; Chondroitin Sulfate Sodium
Dosage : Tablet
Dosage Strength : 500MG; 400MG
Brand Name :
Approval Date :
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Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 500MG
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 500MG
Brand Name :
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : Iran
Brand Name :
Dosage Form : Ointment
Dosage Strength : -
Packaging : 30 G
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Packaging : 30 G
Regulatory Info :
Dosage : Ointment
Dosage Strength : -
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Registration Country : Iran
Regulatory Info :
Registration Country : Serbia
aqua; Lecithin API; Cranberry; Glucosamine Sulphate; Manoseb
Brand Name : Urinosomal Dog
Dosage Form : Syrup
Dosage Strength : 120ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Serbia
Packaging :
Regulatory Info :
aqua; Lecithin API; Cranberry; Glucosamine Sulphate; Manoseb
Dosage : Syrup
Dosage Strength : 120ML
Brand Name : Urinosomal Dog
Approval Date :
Application Number :
Registration Country : Serbia
Regulatory Info :
Registration Country : Turkey
Brand Name : ROTADON
Dosage Form : SACHET
Dosage Strength : 1500MG
Packaging : 20 SACHETS
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Packaging : 20 SACHETS
Regulatory Info :
Dosage : SACHET
Dosage Strength : 1500MG
Brand Name : ROTADON
Approval Date :
Application Number :
Registration Country : Turkey
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ABOUT THIS PAGE
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PharmaCompass offers a list of Glucosamine 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 Glucosamine manufacturer or Glucosamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glucosamine manufacturer or Glucosamine supplier.
PharmaCompass also assists you with knowing the Glucosamine API Price utilized in the formulation of products. Glucosamine API Price is not always fixed or binding as the Glucosamine Price is obtained through a variety of data sources. The Glucosamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levomefolate Glucosamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomefolate Glucosamine, including repackagers and relabelers. The FDA regulates Levomefolate Glucosamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomefolate 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 Levomefolate Glucosamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomefolate Glucosamine supplier is an individual or a company that provides Levomefolate Glucosamine active pharmaceutical ingredient (API) or Levomefolate Glucosamine finished formulations upon request. The Levomefolate Glucosamine suppliers may include Levomefolate Glucosamine API manufacturers, exporters, distributors and traders.
click here to find a list of Levomefolate Glucosamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levomefolate Glucosamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Levomefolate Glucosamine active pharmaceutical ingredient (API) in detail. Different forms of Levomefolate Glucosamine DMFs exist exist since differing nations have different regulations, such as Levomefolate Glucosamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levomefolate Glucosamine DMF submitted to regulatory agencies in the US is known as a USDMF. Levomefolate Glucosamine USDMF includes data on Levomefolate Glucosamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levomefolate Glucosamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Levomefolate 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 Levomefolate Glucosamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Levomefolate 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 Levomefolate 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 Levomefolate Glucosamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levomefolate Glucosamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Levomefolate Glucosamine suppliers with NDC on PharmaCompass.
Levomefolate 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 Levomefolate 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 Levomefolate Glucosamine GMP manufacturer or Levomefolate Glucosamine GMP API supplier for your needs.
A Levomefolate Glucosamine CoA (Certificate of Analysis) is a formal document that attests to Levomefolate Glucosamine's compliance with Levomefolate Glucosamine specifications and serves as a tool for batch-level quality control.
Levomefolate Glucosamine CoA mostly includes findings from lab analyses of a specific batch. For each Levomefolate 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.
Levomefolate Glucosamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Levomefolate Glucosamine EP), Levomefolate Glucosamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levomefolate Glucosamine USP).
