Synopsis
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NDC API
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Data Compilation #PharmaFlow
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1. N-tert-butyl-1-methyl-3,3-diphenylpropylamine
2. N-tert-butyl-3,3-diphenyl-1-methylpropylamine
3. Td 758
4. Td-758
5. Terodiline
1. 7082-21-5
2. Terodiline (hydrochloride)
3. Bicor
4. Terodiline Hydrochloride [usan]
5. K2za89w43f
6. N-t-butyl-1-methyl-3,3-diphenylpropylamine Hydrochloride
7. N-tert-butyl-1-methyl-3,3-diphenylpropylamine Hydrochloride
8. N-tert-butyl-4,4-diphenylbutan-2-amine;hydrochloride
9. Terodiline Chloride
10. N-(tert-butyl)-4,4-diphenylbutan-2-amine Hydrochloride
11. Micturin
12. Micturol
13. Terodiline Hcl
14. Ncgc00183030-01
15. Td-758
16. Unii-k2za89w43f
17. Propylamine, N-tert-butyl-1-methyl-3,3-diphenyl-, Hydrochloride
18. Dsstox_cid_28894
19. Dsstox_rid_83162
20. Dsstox_gsid_48968
21. Mls004712058
22. Chembl539770
23. Dtxsid1048968
24. Chebi:32194
25. Tox21_113412
26. Hy-16489a
27. Terodiline Hydrochloride (jan/usan)
28. Terodiline Hydrochloride [mi]
29. Terodiline Hydrochloride [jan]
30. Benzenepropanamine, N-(1,1-dimethylethyl)-.alpha.-methyl-.gamma.-phenyl-, Hydrochloride
31. Benzenepropanamine, N-(1,1-dimethylethyl)-alpha-methyl-gamma-phenyl-, Hydrochloride
32. Terodiline Hydrochloride [mart.]
33. Terodiline Hydrochloride [who-dd]
34. Smr003475019
35. Cas-7082-21-5
36. Cs-0109448
37. D01873
38. Terodiline Hydrochloride, >=98% (hplc), Solid
39. Q27281873
40. (+/-)-n-tert-butyl-1-methyl-3,3-diphenylpropylamine Hydrochloride
| Molecular Weight | 317.9 g/mol |
|---|---|
| Molecular Formula | C20H28ClN |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Exact Mass | 317.1910276 g/mol |
| Monoisotopic Mass | 317.1910276 g/mol |
| Topological Polar Surface Area | 12 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 261 |
| 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 |
Parasympatholytics
Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS. (See all compounds classified as Parasympatholytics.)
Calcium Channel Blockers
A class of drugs that act by selective inhibition of calcium influx through cellular membranes. (See all compounds classified as Calcium Channel Blockers.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Terodiline 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 Terodiline manufacturer or Terodiline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Terodiline manufacturer or Terodiline supplier.
PharmaCompass also assists you with knowing the Terodiline API Price utilized in the formulation of products. Terodiline API Price is not always fixed or binding as the Terodiline Price is obtained through a variety of data sources. The Terodiline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Terodiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terodiline, including repackagers and relabelers. The FDA regulates Terodiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terodiline 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 Terodiline supplier is an individual or a company that provides Terodiline active pharmaceutical ingredient (API) or Terodiline finished formulations upon request. The Terodiline suppliers may include Terodiline API manufacturers, exporters, distributors and traders.
click here to find a list of Terodiline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Terodiline DMF (Drug Master File) is a document detailing the whole manufacturing process of Terodiline active pharmaceutical ingredient (API) in detail. Different forms of Terodiline DMFs exist exist since differing nations have different regulations, such as Terodiline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Terodiline DMF submitted to regulatory agencies in the US is known as a USDMF. Terodiline USDMF includes data on Terodiline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Terodiline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Terodiline suppliers with USDMF on PharmaCompass.
Terodiline 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 Terodiline 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 Terodiline GMP manufacturer or Terodiline GMP API supplier for your needs.
A Terodiline CoA (Certificate of Analysis) is a formal document that attests to Terodiline's compliance with Terodiline specifications and serves as a tool for batch-level quality control.
Terodiline CoA mostly includes findings from lab analyses of a specific batch. For each Terodiline 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.
Terodiline may be tested according to a variety of international standards, such as European Pharmacopoeia (Terodiline EP), Terodiline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Terodiline USP).
