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1. 9-(n)-et-pronh2-10-des-glynh2-lhrh
2. 9-n-et-pronh2-lhrh
3. Desgly(10)-pro(9)-lhrh Ethylamide
4. Dgnh-lhrh
5. Fertilerine
6. Fertilerine Acetate
7. Fertirelin Acetate
8. Gnrh, (n)-et-pronh2(9)-
9. Gnrh, N-et-pronh2(9)-
10. Lhrh, (n)-et-pronh2(9)-
11. Lhrh, (n)-ethylprolinamide(9)-des-glycinamide(10)-
12. Lhrh, N-et-pronh2(9)-des-gly(10)-
13. Lhrh, N-ethylprolinamide(9)-
14. Tap 031
15. Tap-031
1. 38234-21-8
2. Fertirelina
3. Fertireline
4. Fertirelinum
5. Fertireline [inn-french]
6. Fertirelin [inn:ban]
7. Fertirelinum [inn-latin]
8. Fertirelina [inn-spanish]
9. Unii-q041ao6t91
10. 9-(n-ethyl-l-prolinamide)-10-deglycinamide
11. Fertirelin (inn)
12. Dsstox_cid_31517
13. Dsstox_rid_97402
14. Dsstox_gsid_57728
15. Gtpl9341
16. Chembl3272563
17. Dtxsid8057728
18. Tap 031
19. Tap-031
20. Chebi:177856
21. (des-gly10,pro-nhet9)-lhrh
22. Q041ao6t91
23. Tox21_113925
24. Akos015896030
25. Ncgc00262930-01
26. Cas-38234-21-8
27. D07957
28. A824075
29. Q27286835
30. 9-(n-ethyl-l-prolinamide)-10-deglycinamide Luteinizing Hormone Releasing Factor
| Molecular Weight | 1153.3 g/mol |
|---|---|
| Molecular Formula | C55H76N16O12 |
| XLogP3 | -1 |
| Hydrogen Bond Donor Count | 15 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 30 |
| Exact Mass | 1152.58286192 g/mol |
| Monoisotopic Mass | 1152.58286192 g/mol |
| Topological Polar Surface Area | 432 Ų |
| Heavy Atom Count | 83 |
| Formal Charge | 0 |
| Complexity | 2280 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Fertirelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fertirelin, including repackagers and relabelers. The FDA regulates Fertirelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fertirelin 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 Fertirelin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fertirelin supplier is an individual or a company that provides Fertirelin active pharmaceutical ingredient (API) or Fertirelin finished formulations upon request. The Fertirelin suppliers may include Fertirelin API manufacturers, exporters, distributors and traders.
click here to find a list of Fertirelin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Fertirelin 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 Fertirelin 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 Fertirelin GMP manufacturer or Fertirelin GMP API supplier for your needs.
A Fertirelin CoA (Certificate of Analysis) is a formal document that attests to Fertirelin's compliance with Fertirelin specifications and serves as a tool for batch-level quality control.
Fertirelin CoA mostly includes findings from lab analyses of a specific batch. For each Fertirelin 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.
Fertirelin may be tested according to a variety of international standards, such as European Pharmacopoeia (Fertirelin EP), Fertirelin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fertirelin USP).
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