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1. 2-(2-(diethylamino)ethoxy)ethyl-2-phenylbutyrate Citrate
2. 2-(2-diethylaminoethoxy)ethyl-2-phenylbutamyrate Dihydrogen Citrate
3. Butamirate
4. Butamyrate Citrate
5. Hh 197
6. Sinecod
1. 18109-81-4
2. Abbott 36581
3. Butamirate Citrate [usan]
4. Hh 197
5. Hh-197
6. Abbott-36581
7. Butamirate (citrate)
8. Acodeen
9. Sincodeen
10. Sincodin
11. Sincodix
12. Sinecod
13. 2-(2-(diethylamino)ethoxy)ethyl 2-phenylbutyrate Citrate (1:1)
14. 67hp51l98r
15. 2-[2-(diethylamino)ethoxy]ethyl 2-phenylbutanoate;2-hydroxypropane-1,2,3-tricarboxylic Acid
16. Sincodex
17. Butamirate Citrate (usan)
18. Butamyrate Citrate
19. Dsstox_cid_26270
20. Dsstox_rid_81497
21. Dsstox_gsid_46270
22. Cas-18109-81-4
23. Einecs 242-006-8
24. Unii-67hp51l98r
25. Oxeladin Impurity D
26. 2-(2-(diethylamino)ethoxy)-ethyl 2-phenylbutyrate Citrate
27. Phenyl Acetic Acid Diethylaminoethoxyethanol Ester Citrate
28. 2-phenylbutyric Acid 2-(2-(diethylamino)ethoxy)ethyl Ester Citrate
29. Butamirate-[d5] Citrate
30. Alpha-ethylbenzeneacetic Acid 2-(2-(diethylamino)ethoxy)ethyl Ester Citrate
31. Schembl636120
32. Butamirate Citrate [mi]
33. Chembl2106133
34. Dtxsid0046270
35. Butamirate Citrate [mart.]
36. Bcp22355
37. Butamirate Citrate [who-dd]
38. Tox21_111952
39. Stk069532
40. Akos005390008
41. Diethyl(2-(2-(2-phenylbutyroyloxy)ethoxy)ethyl)ammonium Dihydrogencitrate
42. Tox21_111952_1
43. Butyric Acid, 2-phenyl-, 2-(2-(diethylamino)ethoxy)ethyl Ester, Citrate
44. Ncgc00160645-02
45. Alpha-ethylbenzeneacetic Acid, 2-(2-(diethylamino)ethoxy)ethyl Ester, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
46. Benzeneacetic Acid, Alpha-ethyl-2-(2-(diethylamino)ethoxy)ethyl Ester, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
47. Ft-0663922
48. Ft-0663923
49. D03184
50. J-011560
51. Q27264132
52. Alpha-(ethyl)benzeneacetic Acid 2-[2-(diethylamino)ethoxy]ethyl Ester
53. 2-[2-(diethylamino)ethoxy]ethyl 2-phenylbutanoate 2-hydroxypropane-1,2,3-tricarboxylate (salt)
54. Benzeneacetic Acid, .alpha.-ethyl-2-(2-(diethylamino)ethoxy)ethyl Ester, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
| Molecular Weight | 499.6 g/mol |
|---|---|
| Molecular Formula | C24H37NO10 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 17 |
| Exact Mass | 499.24174638 g/mol |
| Monoisotopic Mass | 499.24174638 g/mol |
| Topological Polar Surface Area | 171 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 513 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
API SUPPLIERS
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EU WC
Date of Issue : 2022-01-05
Valid Till : 2024-06-07
Written Confirmation Number : WC-0422A1
Address of the Firm : Plot No. A-145/8, Khairane, M.1.D.C. Industrial Area, Navi Mumbai-400705, Taluka...
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Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
About the Company : Farmak, A.S. is a privately held chemical and pharmaceutical company based in the Czech Republic. It specializes in researching, developing and producing active pharmaceutical ingr...
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
About the Company : Malladi Drugs & Pharmaceuticals Ltd was founded in 1980 by microbiologist Mr. M L N Sastry. Within a few years, Malladi established itself as a leader in manufacturing ephedrine an...
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...
About the Company : Livmore Life Sciences Pvt. Ltd., established in 2016, is a pharmaceutical company dedicated to the development, optimization, and manufacturing of high-quality Active Pharmaceutica...
About the Company : The company was founded by a technocrat Mr. D. Kesava Reddy in the year 2005. The Managing Director Mr. D. Kesava Reddy along with other three Board of Directors involved in contro...
About the Company : We produce Active Pharmaceutical Ingredients (APIs) providing integrated full-service capabilities. Olon’s ability to develop and manufacture Active Pharmaceutical Ingredients (...
About the Company : SAI-TECH PHARMACEUTICALS PRIVATE LIMITED is dedicated Active Pharmaceutical Ingredients (API) manufacturing company for producing & providing high quality products as per customer ...
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INTERMEDIATE SUPPLIERS
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Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : Syrup
Dosage Strength : 7.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info :
Registration Country : Sweden
Brand Name : Tinguri
Dosage Form : SYRUP
Dosage Strength : 1.5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Turkey
Brand Name : TUSAMOL
Dosage Form : Syrup
Dosage Strength : 7.5MG/5ML
Packaging : 100 ml Glass Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info :
Registration Country : Ukraine
butamirate citrate; Guaifenesin
Brand Name : Pectolvan STOP
Dosage Form : Oral Drops
Dosage Strength :
Packaging : 25ML Glass Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Ukraine
Regulatory Info :
Registration Country : Poland
Brand Name : Natussic
Dosage Form : Syrup
Dosage Strength : 7.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Poland
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Regulatory Info :
Registration Country : Sweden
Brand Name : Tinguri
Dosage Form : SYRUP
Dosage Strength : 1.5 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Ukraine
butamirate citrate; Guaifenesin
Brand Name : Pectolvan STOP
Dosage Form : Oral Drops
Dosage Strength :
Packaging : 25ML Glass Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Ukraine
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Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : Syrup
Dosage Strength : 7.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Packaging :
Regulatory Info : Generic
Dosage : Syrup
Dosage Strength : 7.5MG/5ML
Brand Name :
Approval Date :
Application Number :
Registration Country : Turkey
Regulatory Info :
Registration Country : Turkey
Brand Name : TUSAMOL
Dosage Form : Syrup
Dosage Strength : 7.5MG/5ML
Packaging : 100 ml Glass Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Packaging : 100 ml Glass Bottle
Regulatory Info :
Dosage : Syrup
Dosage Strength : 7.5MG/5ML
Brand Name : TUSAMOL
Approval Date :
Application Number :
Registration Country : Turkey
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ABOUT THIS PAGE
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PharmaCompass offers a list of Butamirate Citrate 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 Butamirate Citrate manufacturer or Butamirate Citrate supplier for your needs.
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PharmaCompass also assists you with knowing the Butamirate Citrate API Price utilized in the formulation of products. Butamirate Citrate API Price is not always fixed or binding as the Butamirate Citrate Price is obtained through a variety of data sources. The Butamirate Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sinecod manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sinecod, including repackagers and relabelers. The FDA regulates Sinecod manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sinecod 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 Sinecod manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sinecod supplier is an individual or a company that provides Sinecod active pharmaceutical ingredient (API) or Sinecod finished formulations upon request. The Sinecod suppliers may include Sinecod API manufacturers, exporters, distributors and traders.
click here to find a list of Sinecod suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sinecod written confirmation (Sinecod WC) is an official document issued by a regulatory agency to a Sinecod manufacturer, verifying that the manufacturing facility of a Sinecod active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sinecod APIs or Sinecod finished pharmaceutical products to another nation, regulatory agencies frequently require a Sinecod WC (written confirmation) as part of the regulatory process.
click here to find a list of Sinecod suppliers with Written Confirmation (WC) on PharmaCompass.
Sinecod 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 Sinecod 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 Sinecod GMP manufacturer or Sinecod GMP API supplier for your needs.
A Sinecod CoA (Certificate of Analysis) is a formal document that attests to Sinecod's compliance with Sinecod specifications and serves as a tool for batch-level quality control.
Sinecod CoA mostly includes findings from lab analyses of a specific batch. For each Sinecod 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.
Sinecod may be tested according to a variety of international standards, such as European Pharmacopoeia (Sinecod EP), Sinecod JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sinecod USP).
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