Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 1224690-84-9
2. 4b136gsg9m
3. 7-((3-chloro-6-methyl-5,5-dioxido-6,11-dihydrodibenzo[c,f][1,2]thiazepin-11-yl)amino)heptanoic Acid Compound With Sulfuric Acid (2:1) Dihydrate
4. Tianeptine Hemisulfate Monohydrate (thm)
5. Heptanoic Acid, 7-((3-chloro-6,11-dihydro-6-methyl-5,5-dioxidodibenzo(c,f)(1,2)thiazepin-11-yl)amino)-, Sulfate, Hydrate (2:1:2)
6. Unii-4b136gsg9m
7. Tianeptine Sulfate;tianeptine-d4
8. Bcp30653
9. Ex-a2725
10. A902166
11. Q27259365
12. 7-[(3-chloro-6,11-dihydro-6-methyl-5,5-dioxidodibenzo[c,f][1,2]thiazepin-11-yl)amino]heptanoic Acid Sulfate Hydrate (2:1:2)
Molecular Weight | 1008.0 g/mol |
---|---|
Molecular Formula | C42H56Cl2N4O14S3 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 18 |
Rotatable Bond Count | 16 |
Exact Mass | 1006.2332214 g/mol |
Monoisotopic Mass | 1006.2332214 g/mol |
Topological Polar Surface Area | 275 Ų |
Heavy Atom Count | 65 |
Formal Charge | 0 |
Complexity | 735 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 5 |
ABOUT THIS PAGE
A Tianeptine Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tianeptine Sulphate, including repackagers and relabelers. The FDA regulates Tianeptine Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tianeptine Sulphate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tianeptine Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tianeptine Sulphate supplier is an individual or a company that provides Tianeptine Sulphate active pharmaceutical ingredient (API) or Tianeptine Sulphate finished formulations upon request. The Tianeptine Sulphate suppliers may include Tianeptine Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Tianeptine Sulphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Tianeptine Sulphate 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 Tianeptine Sulphate 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 Tianeptine Sulphate GMP manufacturer or Tianeptine Sulphate GMP API supplier for your needs.
A Tianeptine Sulphate CoA (Certificate of Analysis) is a formal document that attests to Tianeptine Sulphate's compliance with Tianeptine Sulphate specifications and serves as a tool for batch-level quality control.
Tianeptine Sulphate CoA mostly includes findings from lab analyses of a specific batch. For each Tianeptine Sulphate 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.
Tianeptine Sulphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Tianeptine Sulphate EP), Tianeptine Sulphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tianeptine Sulphate USP).
LOOKING FOR A SUPPLIER?