Synopsis
Synopsis
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CEP/COS
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JDMF
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NDC API
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1. 200880-42-8
2. 1,2-distearoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt
3. 1,2-dioctadecanoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt)
4. Sodium;2,3-dihydroxypropyl [(2r)-2,3-di(octadecanoyloxy)propyl] Phosphate
5. 1,2-distearoyl-sn-glycero-3-phosphoglycerol
6. 771667q09x
7. Octadecanoic Acid, 1,1'-((1r)-1-((((2,3-dihydroxypropoxy)hydroxyphosphinyl)oxy)methyl)-1,2-ethanediyl) Ester, Sodium Salt (1:1)
8. 1,2-distearoyl-sn-glycero-3-phospho-rac-glycerol Sodium Salt
9. 1,2-distearoyl-sn-glycero-3-phosphatidylglycerol (sodium)
10. Sodium 1,2-distearoyl-sn-glycero-3-phospho-(1'-rac-glycerol)
11. 67232-82-0
12. 1,2-dioctadecanoyl-sn-glycero-3-phospho-(1'-rac-glycerol) Sodium Salt
13. Dspg-na
14. Unii-771667q09x
15. 1,2-distearoyl-sn-glycero-3-phosphoglycerol,sodium Salt
16. Dspg-na, L-
17. Dspg-na, R-
18. Dtxsid80173908
19. Mfcd00077290
20. Akos015833420
21. Bp-26317
22. Hy-145742
23. Cs-0380628
24. D5648
25. E78022
26. J-013003
27. Q27266534
28. 1,2-distearoyl-sn-glycero-3-phosphoglycerol, Sodium Salt
29. Sodium (r)-2,3-bis(stearoyloxy)propyl 2,3-dihydroxypropyl Phosphate
30. 1,2-dioctadecanoyl-sn-glycero-3-phospho-(1'-rac-glycerol) Monosodium Salt
31. Sodium (r)-2,3-bis(stearoyloxy)propyl (2,3-dihydroxypropyl) Phosphate
32. 1,2-distearoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt, >=97.0% (tlc)
33. 1-o,2-o-distearoyl-3-o-[2,3-dihydroxypropoxy(sodiooxy)phosphinyl]-l-glycerol
| Molecular Weight | 801.1 g/mol |
|---|---|
| Molecular Formula | C42H82NaO10P |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 44 |
| Exact Mass | 800.55433009 g/mol |
| Monoisotopic Mass | 800.55433009 g/mol |
| Topological Polar Surface Area | 152 Ų |
| Heavy Atom Count | 54 |
| Formal Charge | 0 |
| Complexity | 865 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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USDMF
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Average Price (USD/KGS) |
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ABOUT THIS PAGE
A DSPG manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSPG, including repackagers and relabelers. The FDA regulates DSPG manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSPG API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A DSPG supplier is an individual or a company that provides DSPG active pharmaceutical ingredient (API) or DSPG finished formulations upon request. The DSPG suppliers may include DSPG API manufacturers, exporters, distributors and traders.
click here to find a list of DSPG suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSPG DMF (Drug Master File) is a document detailing the whole manufacturing process of DSPG active pharmaceutical ingredient (API) in detail. Different forms of DSPG DMFs exist exist since differing nations have different regulations, such as DSPG USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSPG DMF submitted to regulatory agencies in the US is known as a USDMF. DSPG USDMF includes data on DSPG's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSPG USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DSPG suppliers with USDMF on PharmaCompass.
DSPG 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 DSPG 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 DSPG GMP manufacturer or DSPG GMP API supplier for your needs.
A DSPG CoA (Certificate of Analysis) is a formal document that attests to DSPG's compliance with DSPG specifications and serves as a tool for batch-level quality control.
DSPG CoA mostly includes findings from lab analyses of a specific batch. For each DSPG 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.
DSPG may be tested according to a variety of international standards, such as European Pharmacopoeia (DSPG EP), DSPG JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSPG USP).
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