Synopsis
Synopsis
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CEP/COS
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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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EDQM
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USP
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JP
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Others
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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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US Exclusivities
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Health Canada Patents
US Medicaid
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Data Compilation #PharmaFlow
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1. Hydrochloride, Methaqualone
2. Methaqualone
3. Metolquizolone
4. Optimil
5. Ortonal
6. Quaalude
1. Melsedin
2. Somnofac
3. Mequal
4. Optimil
5. Parest
6. 340-56-7
7. Methaqualone Hcl
8. Melsed Hcl
9. Mtq Hydrochloride
10. Sopor Hydrochloride
11. Somnafac
12. Quaalude Hydrochloride
13. Hyminal Monohydrochloride
14. Tr 495 Monohydrochloride
15. Methylquinazolone Hydrochloride
16. Nsc-75892
17. Rjq4g25zrh
18. 2-methyl-3-(o-tolyl)-4-quinazolone Hydrochloride
19. 4(3h)-quinazolinone, 2-methyl-3-(2-methylphenyl)-, Monohydrochloride
20. 2-methyl-3-tolylchinazolon-4 Hydrochloride
21. 2915-01-7
22. 2-methyl-3-(2-methylphenyl)quinazolin-4-one Hydrochloride
23. Mozambin Hydrochloride
24. 2-methyl-3-(2-methylphenyl)quinazolin-4-one;hydrochloride
25. Einecs 206-431-2
26. Unii-rjq4g25zrh
27. Nsc 75892
28. Chi 38
29. Methaqualone Hydrochloride [usp]
30. Qz 2 Hydrochloride
31. 2-methyl-3-tolylchinazolon-4 Hydrochloride [german]
32. 2-methyl-3-o-tolyl-4(3h)-quinazolinone Hydrochloride
33. 2-methyl-3-o-tolyl-4(3h)-quinazolinone Monohydrochloride
34. 2-metil-3-(o-tolil)-4-chinazolone Chloridrato [italian]
35. 4(3h)-quinazolinone, 2-methyl-3-o-tolyl-, Hydrochloride
36. 2-metil-3-(o-tolil)-4-chinazolone Chloridrato
37. Schembl3500629
38. Chembl2106829
39. Dtxsid10951751
40. 4(3h)-quinazolinone, 2-methyl-3-o-tolyl-, Monohydrochloride
41. Nsc75892
42. 4(3h)-quinazolinone, Hydrochloride
43. 2-methyl-3-(2'-trifluormethylphenyl) Chinazolon-4 Hydrochloride [german]
44. 4(3h)-quinazolinone, 2-methyl-3-(o-trifluoromethylphenyl)-, Hydrochloride
45. Akos027439985
46. 4(3h)-quinazolinone, Monohydrochloride
47. Methaqualone Hydrochloride [mi]
48. Methaqualone Hydrochloride [who-dd]
49. Wln: T66 Bvn Enj Cr B1 & D1
50. Ft-0603381
51. Q27288151
52. 2-methyl-3-(2'-trifluormethylphenyl) Chinazolon-4 Hydrochloride
53. 2-methyl-3-(2-methylphenyl)quinazolin-4(3h)-one--hydrogen Chloride (1/1)
| Molecular Weight | 286.75 g/mol |
|---|---|
| Molecular Formula | C16H15ClN2O |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 286.0872908 g/mol |
| Monoisotopic Mass | 286.0872908 g/mol |
| Topological Polar Surface Area | 32.7 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 390 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Hypnotics and Sedatives
Drugs used to induce drowsiness or sleep or to reduce psychological excitement or anxiety. (See all compounds classified as Hypnotics and Sedatives.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Methaqualone 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 Methaqualone manufacturer or Methaqualone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methaqualone manufacturer or Methaqualone supplier.
PharmaCompass also assists you with knowing the Methaqualone API Price utilized in the formulation of products. Methaqualone API Price is not always fixed or binding as the Methaqualone Price is obtained through a variety of data sources. The Methaqualone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quaalude manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quaalude, including repackagers and relabelers. The FDA regulates Quaalude manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quaalude 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 Quaalude supplier is an individual or a company that provides Quaalude active pharmaceutical ingredient (API) or Quaalude finished formulations upon request. The Quaalude suppliers may include Quaalude API manufacturers, exporters, distributors and traders.
click here to find a list of Quaalude suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Quaalude DMF (Drug Master File) is a document detailing the whole manufacturing process of Quaalude active pharmaceutical ingredient (API) in detail. Different forms of Quaalude DMFs exist exist since differing nations have different regulations, such as Quaalude USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Quaalude DMF submitted to regulatory agencies in the US is known as a USDMF. Quaalude USDMF includes data on Quaalude's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Quaalude USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Quaalude suppliers with USDMF on PharmaCompass.
Quaalude 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 Quaalude 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 Quaalude GMP manufacturer or Quaalude GMP API supplier for your needs.
A Quaalude CoA (Certificate of Analysis) is a formal document that attests to Quaalude's compliance with Quaalude specifications and serves as a tool for batch-level quality control.
Quaalude CoA mostly includes findings from lab analyses of a specific batch. For each Quaalude 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.
Quaalude may be tested according to a variety of international standards, such as European Pharmacopoeia (Quaalude EP), Quaalude JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Quaalude USP).
