Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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API
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FDF
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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Others
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US Patents
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US Exclusivities
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US Medicaid
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Annual Reports
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Finished Drug Prices
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1. Popg Na, L-
2. Popg Na, R-
3. Popg-na, L-
4. Popg-na, R-
5. 268550-95-4
6. 202070-86-8
7. T52ti8bmq6
8. 1-palmitoyl-2-oleoyl-phosphatidyl-glycerol Sodium
9. Sodium;2,3-dihydroxypropyl [(2r)-3-hexadecanoyloxy-2-[(z)-octadec-9-enoyl]oxypropyl] Phosphate
10. 383907-64-0
11. 1-palmitoyl-2-oleoyl-sn-glycero-3-(phospho-rac-(1-glycerol)), Sodium Salt
12. 9-octadecenoic Acid (9z)-, (1r)-1-((((2,3-dihydroxypropoxy)hydroxyphosphinyl)oxy)methyl)-2-((1-oxohexadecyl)oxy)ethyl Ester, Sodium Salt (1:1)
13. Sodium 2,3-dihydroxypropyl ((2r)-3-hexadecanoyloxy-2-((z)-octadec-9-enoyl)oxy-propyl) Phosphate
14. Sodium 1-palmitoyl-2-oleoyl-sn-glycero-3-(phospho-rac-(1-glycerol))
15. 1-palmitoyl-2-oleyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt
16. Sodium 2,3-dihydroxypropyl ((r)-2-(oleoyloxy)-3-(palmitoyloxy)propyl) Phosphate(z)
17. 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt)
18. Unii-t52ti8bmq6
19. Epg-na
20. Popg-na
21. Starbld0000181
22. 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-sn-1-glycerol Sodium Salt
23. L-a-phosphatidylglycerols (egg)
24. Surfaxin Component Popg, Na
25. Mfcd00674290
26. Lucinactant Component Popg, Na
27. Bp-26321
28. Bp-26334
29. Hy-130463
30. Cs-0108062
31. T72199
32. J-016573
33. Non-hydrogenated Egg Phosphatidylglycerol, Sodium Salt
34. Q27289682
35. Egg Pg, L-alpha-phosphatidylglycerol (egg, Chicken) (sodium Salt), Powder
36. 2-oleoyl-1-palmitoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt, >=98.0% (tlc)
37. Egg Pg, L-alpha-phosphatidylglycerol (egg, Chicken) (sodium Salt), Chloroform
38. (2r)-1-(((2,3-dihydroxypropoxy)(hydroxy)phosphoryl)oxy)-3-(palmitoyloxy)propan-2-yl Oleate, Sodium Salt(1:x)
39. 16:0-18:1 Pg, 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium Salt), Powder
40. Phosphoric Acid Sodium 2,3-dihydroxypropyl[(2r)-2-(oleoyloxy)-3-(palmitoyloxy)propyl] Ester Salt
| Molecular Weight | 771.0 g/mol |
|---|---|
| Molecular Formula | C40H76NaO10P |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 41 |
| Exact Mass | 770.50737990 g/mol |
| Monoisotopic Mass | 770.50737990 g/mol |
| Topological Polar Surface Area | 152 Ų |
| Heavy Atom Count | 52 |
| Formal Charge | 0 |
| Complexity | 875 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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ABOUT THIS PAGE
A POPG manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of POPG, including repackagers and relabelers. The FDA regulates POPG manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. POPG 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 POPG supplier is an individual or a company that provides POPG active pharmaceutical ingredient (API) or POPG finished formulations upon request. The POPG suppliers may include POPG API manufacturers, exporters, distributors and traders.
click here to find a list of POPG suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A POPG DMF (Drug Master File) is a document detailing the whole manufacturing process of POPG active pharmaceutical ingredient (API) in detail. Different forms of POPG DMFs exist exist since differing nations have different regulations, such as POPG USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A POPG DMF submitted to regulatory agencies in the US is known as a USDMF. POPG USDMF includes data on POPG's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The POPG USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of POPG suppliers with USDMF on PharmaCompass.
POPG 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 POPG 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 POPG GMP manufacturer or POPG GMP API supplier for your needs.
A POPG CoA (Certificate of Analysis) is a formal document that attests to POPG's compliance with POPG specifications and serves as a tool for batch-level quality control.
POPG CoA mostly includes findings from lab analyses of a specific batch. For each POPG 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.
POPG may be tested according to a variety of international standards, such as European Pharmacopoeia (POPG EP), POPG JP (Japanese Pharmacopeia) and the US Pharmacopoeia (POPG USP).
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