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1. Tinlarebant [usan]
2. Lbs-008
3. Bpn-14967
4. 63wi9s8p1m
5. 1-(3-(4-(3,4-difluoro-2-(trifluoromethyl)phenyl)piperidine-1-carbonyl)-1h,4h,5h,6h,7h-pyrazolo(3,4-c)pyridin-6-yl)ethan-1-one
6. 1821327-95-0
7. Ethanone, 1-(3-((4-(3,4-difluoro-2-(trifluoromethyl)phenyl)-1-piperidinyl)carbonyl)-1,4,5,7-tetrahydro-6h-pyrazolo(3,4-c)pyridin-6-yl)
8. Tinlarebant [inn]
9. Unii-63wi9s8p1m
10. Chembl3967849
11. Schembl17223028
12. Bdbm249482
13. Who 11058
14. Us9434727, 80
15. Us9434727, 81
16. 1-(3-(4-(3,4-difluoro-2-(trifluoromethyl)phenyl)piperidine-1-carbonyl)-4,5-dihydro-1h-pyrazolo[3,4-c]pyridin-6(7h)-yl)ethanone
| Molecular Weight | 456.4 g/mol |
|---|---|
| Molecular Formula | C21H21F5N4O2 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 2 |
| Exact Mass | 456.15846674 g/mol |
| Monoisotopic Mass | 456.15846674 g/mol |
| Topological Polar Surface Area | 69.3 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 715 |
| 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 | 1 |
Drugs in Development
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PharmaCompass offers a list of Tinlarebant 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 Tinlarebant manufacturer or Tinlarebant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tinlarebant manufacturer or Tinlarebant supplier.
PharmaCompass also assists you with knowing the Tinlarebant API Price utilized in the formulation of products. Tinlarebant API Price is not always fixed or binding as the Tinlarebant Price is obtained through a variety of data sources. The Tinlarebant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tinlarebant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tinlarebant, including repackagers and relabelers. The FDA regulates Tinlarebant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tinlarebant 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 Tinlarebant supplier is an individual or a company that provides Tinlarebant active pharmaceutical ingredient (API) or Tinlarebant finished formulations upon request. The Tinlarebant suppliers may include Tinlarebant API manufacturers, exporters, distributors and traders.
Tinlarebant 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 Tinlarebant 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 Tinlarebant GMP manufacturer or Tinlarebant GMP API supplier for your needs.
A Tinlarebant CoA (Certificate of Analysis) is a formal document that attests to Tinlarebant's compliance with Tinlarebant specifications and serves as a tool for batch-level quality control.
Tinlarebant CoA mostly includes findings from lab analyses of a specific batch. For each Tinlarebant 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.
Tinlarebant may be tested according to a variety of international standards, such as European Pharmacopoeia (Tinlarebant EP), Tinlarebant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tinlarebant USP).
