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1. Alkaloids, Hydrogenated Ergot
2. Co-dergocrine
3. Dihydroergotoxin
4. Ergot Alkaloids, Hydrogenated
5. Hydrogenated Ergot Alkaloids
1. 11032-41-0
2. 6190-39-2
3. Dihydroergotamine Methanesulfonate Salt
4. (6ar,9r)-n-[(1s,2s,4r,7s)-7-benzyl-2-hydroxy-4-methyl-5,8-dioxo-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9,10,10a-hexahydro-4h-indolo[4,3-fg]quinoline-9-carboxamide;methanesulfonic Acid
5. Smr001230668
6. Prestwick_746
7. Schembl40844
8. Mls002153175
9. Mls002207048
10. Chembl1396675
11. Hms2231h03
12. Hms3886k22
13. Dihydroergotamine For Peak Identification
14. D2633
15. Dihydroergotamine Methanesulfonate Salt, Powder
16. Q16633838
17. Z1544404034
18. Dihydroergotamine Mesilate, European Pharmacopoeia (ep) Reference Standard
19. Dihydroergotamine For Peak Identification, European Pharmacopoeia (ep) Reference Standard
20. Dihydroergotamine Mesylate, United States Pharmacopeia (usp) Reference Standard
21. (4r,7r)-n-[(1s,2s,4r,7s)-7-benzyl-2-hydroxy-4-methyl-5,8-dioxo-3-oxa-6,9-diazatricyclo[7.3.0.0^{2,6}]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(15),9,12(16),13-tetraene-4-carboxamide; Methanesulfonic Acid
22. (6ar,9r)-n-((2r,5s,10as,10bs)-5-benzyl-10b-hydroxy-2-methyl-3,6-dioxooctahydro-2h-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-7-methyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxamide
23. (6ar,9r)-n-((2r,5s,10as,10bs)-5-benzyl-10b-hydroxy-2-methyl-3,6-dioxooctahydro-2h-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-7-methyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxamide Methanesulfonate
24. (6ar,9r)-n-((2r,5s,10as,10bs)-5-benzyl-10b-hydroxy-2-methyl-3,6-dioxooctahydro-8h-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-7-methyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxamide Methanesulfonate
25. 910882-41-6
Molecular Weight | 679.8 g/mol |
---|---|
Molecular Formula | C34H41N5O8S |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 9 |
Rotatable Bond Count | 4 |
Exact Mass | 679.26758446 g/mol |
Monoisotopic Mass | 679.26758446 g/mol |
Topological Polar Surface Area | 181 Ų |
Heavy Atom Count | 48 |
Formal Charge | 0 |
Complexity | 1260 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
1 of 2 | |
---|---|
Drug Name | Dihydroergotamine mesylate |
Active Ingredient | Dihydroergotamine mesylate |
Dosage Form | Injectable |
Route | Injection |
Strength | 1mg/ml |
Market Status | Prescription |
Company | Paddock; Bedford Labs |
2 of 2 | |
---|---|
Drug Name | Dihydroergotamine mesylate |
Active Ingredient | Dihydroergotamine mesylate |
Dosage Form | Injectable |
Route | Injection |
Strength | 1mg/ml |
Market Status | Prescription |
Company | Paddock; Bedford Labs |
Adrenergic alpha-Antagonists
Drugs that bind to but do not activate alpha-adrenergic receptors thereby blocking the actions of endogenous or exogenous adrenergic agonists. Adrenergic alpha-antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma. (See all compounds classified as Adrenergic alpha-Antagonists.)
Dopamine Agonists
Drugs that bind to and activate dopamine receptors. (See all compounds classified as Dopamine Agonists.)
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PharmaCompass offers a list of Dihydroergotamine Mesylate 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 Dihydroergotamine Mesylate manufacturer or Dihydroergotamine Mesylate supplier for your needs.
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A Aliud Brand of Dihydroergotamine Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aliud Brand of Dihydroergotamine Mesylate, including repackagers and relabelers. The FDA regulates Aliud Brand of Dihydroergotamine Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aliud Brand of Dihydroergotamine Mesylate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Aliud Brand of Dihydroergotamine Mesylate supplier is an individual or a company that provides Aliud Brand of Dihydroergotamine Mesylate active pharmaceutical ingredient (API) or Aliud Brand of Dihydroergotamine Mesylate finished formulations upon request. The Aliud Brand of Dihydroergotamine Mesylate suppliers may include Aliud Brand of Dihydroergotamine Mesylate API manufacturers, exporters, distributors and traders.
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A Aliud Brand of Dihydroergotamine Mesylate DMF (Drug Master File) is a document detailing the whole manufacturing process of Aliud Brand of Dihydroergotamine Mesylate active pharmaceutical ingredient (API) in detail. Different forms of Aliud Brand of Dihydroergotamine Mesylate DMFs exist exist since differing nations have different regulations, such as Aliud Brand of Dihydroergotamine Mesylate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aliud Brand of Dihydroergotamine Mesylate DMF submitted to regulatory agencies in the US is known as a USDMF. Aliud Brand of Dihydroergotamine Mesylate USDMF includes data on Aliud Brand of Dihydroergotamine Mesylate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aliud Brand of Dihydroergotamine Mesylate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A Aliud Brand of Dihydroergotamine Mesylate CEP of the European Pharmacopoeia monograph is often referred to as a Aliud Brand of Dihydroergotamine Mesylate Certificate of Suitability (COS). The purpose of a Aliud Brand of Dihydroergotamine Mesylate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aliud Brand of Dihydroergotamine Mesylate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aliud Brand of Dihydroergotamine Mesylate to their clients by showing that a Aliud Brand of Dihydroergotamine Mesylate CEP has been issued for it. The manufacturer submits a Aliud Brand of Dihydroergotamine Mesylate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aliud Brand of Dihydroergotamine Mesylate CEP holder for the record. Additionally, the data presented in the Aliud Brand of Dihydroergotamine Mesylate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aliud Brand of Dihydroergotamine Mesylate DMF.
A Aliud Brand of Dihydroergotamine Mesylate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aliud Brand of Dihydroergotamine Mesylate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Aliud Brand of Dihydroergotamine Mesylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aliud Brand of Dihydroergotamine Mesylate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Aliud Brand of Dihydroergotamine Mesylate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Aliud Brand of Dihydroergotamine Mesylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aliud Brand of Dihydroergotamine Mesylate NDC to their finished compounded human drug products, they may choose to do so.
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Aliud Brand of Dihydroergotamine Mesylate 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 Aliud Brand of Dihydroergotamine Mesylate 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 Aliud Brand of Dihydroergotamine Mesylate GMP manufacturer or Aliud Brand of Dihydroergotamine Mesylate GMP API supplier for your needs.
A Aliud Brand of Dihydroergotamine Mesylate CoA (Certificate of Analysis) is a formal document that attests to Aliud Brand of Dihydroergotamine Mesylate's compliance with Aliud Brand of Dihydroergotamine Mesylate specifications and serves as a tool for batch-level quality control.
Aliud Brand of Dihydroergotamine Mesylate CoA mostly includes findings from lab analyses of a specific batch. For each Aliud Brand of Dihydroergotamine Mesylate 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.
Aliud Brand of Dihydroergotamine Mesylate may be tested according to a variety of international standards, such as European Pharmacopoeia (Aliud Brand of Dihydroergotamine Mesylate EP), Aliud Brand of Dihydroergotamine Mesylate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aliud Brand of Dihydroergotamine Mesylate USP).