Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. 2,4,6(1h,3h,5h)-pyrimidinetrione, 5-ethyl-5-(1-methylpropyl)-, Monosodium Salt
2. Butabarbital
3. Butabarbital Sodium
4. Butabarbitone
5. Butisol
6. Butisol Sodium
7. Sarisol
8. Secbutabarbital
9. Secbutabarbital Sodium
10. Secbutobarbitone
11. Secumalum
1. Butabarbital Sodium
2. Carrbutabarb
3. Expansatol
4. Asturidon
5. Barbitab
6. Bubartal
7. Butalan
8. Butasaron
9. Butased
10. Butazem
11. Cambrised
12. Ciprial
13. Insolat
14. Intasedol
15. Loubarb
16. Mebutal
17. Neravan
18. Noctinal
19. Prelital
20. Quiebar
21. Butak
22. Butatal Sodium
23. Butisol Sodium
24. Butabarpal Sodium
25. Bubartal Tt
26. Seda-bute
27. Sodium Butabarbital
28. Butabarbitone Sodium
29. Secbubarbital Sodium
30. Sodium Butobarbitone
31. 143-81-7
32. Secbutobarbitone Sodium
33. Sodium;5-butan-2-yl-5-ethyl-1,3-diazinane-2,4,6-trione
34. Sodium 5-ethyl-5-sec-butylbarbiturate
35. Sodium 5-sec-butyl-5-ethylbarbiturate
36. Wln: T6vmvmv Fhj Fy2 & 1 F2
37. Sodium 5-ethyl-5-(1-methylpropyl)barbiturate
38. Component Of Butibel
39. Nsc11778
40. 5-sec-butyl-5-ethylbarbituric Acid, Sodium Salt
41. 5-sec-butyl-5-ethyl-barbituric Acid, Na Salt
42. 5-ethyl-5-(1-methylpropyl)barbituric Acid, Sodium Salt
43. 2,6(1h,3h,5h)-pyrimidinetrione, 5-ethyl-5-(1-methylpropyl)-, Monosodium Salt
Molecular Weight | 235.24 g/mol |
---|---|
Molecular Formula | C10H16N2NaO3+ |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 3 |
Exact Mass | 235.10586166 g/mol |
Monoisotopic Mass | 235.10586166 g/mol |
Topological Polar Surface Area | 75.3 Ų |
Heavy Atom Count | 16 |
Formal Charge | 1 |
Complexity | 292 |
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 |
1 of 2 | |
---|---|
Drug Name | Butisol sodium |
PubMed Health | Butabarbital (By mouth) |
Drug Classes | Sedative |
Drug Label | BUTISOL SODIUM (butabarbital sodium tablets, USP and butabarbital sodium oral solution, USP) is a non-selective central nervous system depressant which is used as a sedative or hypnotic. It is available for oral administration as Tablets containing... |
Active Ingredient | Butabarbital sodium |
Dosage Form | Elixir; Tablet |
Route | Oral |
Strength | 30mg/5ml; 50mg; 30mg |
Market Status | Prescription |
Company | Meda Pharms |
2 of 2 | |
---|---|
Drug Name | Butisol sodium |
PubMed Health | Butabarbital (By mouth) |
Drug Classes | Sedative |
Drug Label | BUTISOL SODIUM (butabarbital sodium tablets, USP and butabarbital sodium oral solution, USP) is a non-selective central nervous system depressant which is used as a sedative or hypnotic. It is available for oral administration as Tablets containing... |
Active Ingredient | Butabarbital sodium |
Dosage Form | Elixir; Tablet |
Route | Oral |
Strength | 30mg/5ml; 50mg; 30mg |
Market Status | Prescription |
Company | Meda Pharms |
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
68
PharmaCompass offers a list of Paxital 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 Paxital manufacturer or Paxital supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paxital manufacturer or Paxital supplier.
PharmaCompass also assists you with knowing the Paxital API Price utilized in the formulation of products. Paxital API Price is not always fixed or binding as the Paxital Price is obtained through a variety of data sources. The Paxital Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paxital manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paxital, including repackagers and relabelers. The FDA regulates Paxital manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paxital 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 Paxital supplier is an individual or a company that provides Paxital active pharmaceutical ingredient (API) or Paxital finished formulations upon request. The Paxital suppliers may include Paxital API manufacturers, exporters, distributors and traders.
Paxital 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 Paxital 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 Paxital GMP manufacturer or Paxital GMP API supplier for your needs.
A Paxital CoA (Certificate of Analysis) is a formal document that attests to Paxital's compliance with Paxital specifications and serves as a tool for batch-level quality control.
Paxital CoA mostly includes findings from lab analyses of a specific batch. For each Paxital 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.
Paxital may be tested according to a variety of international standards, such as European Pharmacopoeia (Paxital EP), Paxital JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Paxital USP).