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1. 4,4-diphenyl-1-tert-butylpiperidine Hydrochloride
2. Budipine
3. Parkinsan
1. 63661-61-0
2. Parkinsan
3. Budipine (hydrochloride)
4. Nbf4q9307q
5. 1-tert-butyl-4,4-diphenylpiperidinium Chloride
6. Budipine Hcl
7. 1-tert-butyl-4,4-diphenylpiperidine;hydrochloride
8. Unii-nbf4q9307q
9. Parkinsan (tn)
10. Einecs 264-388-5
11. 1-tert-butyl-4,4-diphenylpiperidine Hydrochloride
12. Schembl1506558
13. Niosh/tm5031200
14. Budipine Hydrochloride [mi]
15. By-701
16. Budipine Hydrochloride [who-dd]
17. Tm50312000
18. D07589
19. 1-t-butyl-4,4-di-phenyl-piperidine-hydrochloride
20. Q27284776
21. Piperidine, 1-tert-butyl-4,4-diphenyl-, Hydrochloride
| Molecular Weight | 329.9 g/mol |
|---|---|
| Molecular Formula | C21H28ClN |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 329.1910276 g/mol |
| Monoisotopic Mass | 329.1910276 g/mol |
| Topological Polar Surface Area | 3.2 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 313 |
| 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 |
Antiparkinson Agents
Agents used in the treatment of Parkinson's disease. The most commonly used drugs act on the dopaminergic system in the striatum and basal ganglia or are centrally acting muscarinic antagonists. (See all compounds classified as Antiparkinson Agents.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Budipine 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 Budipine manufacturer or Budipine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Budipine manufacturer or Budipine supplier.
PharmaCompass also assists you with knowing the Budipine API Price utilized in the formulation of products. Budipine API Price is not always fixed or binding as the Budipine Price is obtained through a variety of data sources. The Budipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Budipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Budipine, including repackagers and relabelers. The FDA regulates Budipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Budipine 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 Budipine supplier is an individual or a company that provides Budipine active pharmaceutical ingredient (API) or Budipine finished formulations upon request. The Budipine suppliers may include Budipine API manufacturers, exporters, distributors and traders.
click here to find a list of Budipine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Budipine DMF (Drug Master File) is a document detailing the whole manufacturing process of Budipine active pharmaceutical ingredient (API) in detail. Different forms of Budipine DMFs exist exist since differing nations have different regulations, such as Budipine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Budipine DMF submitted to regulatory agencies in the US is known as a USDMF. Budipine USDMF includes data on Budipine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Budipine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Budipine suppliers with USDMF on PharmaCompass.
Budipine 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 Budipine 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 Budipine GMP manufacturer or Budipine GMP API supplier for your needs.
A Budipine CoA (Certificate of Analysis) is a formal document that attests to Budipine's compliance with Budipine specifications and serves as a tool for batch-level quality control.
Budipine CoA mostly includes findings from lab analyses of a specific batch. For each Budipine 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.
Budipine may be tested according to a variety of international standards, such as European Pharmacopoeia (Budipine EP), Budipine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Budipine USP).
