Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
EDQM
0
USP
0
JP
0
Others
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
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidin-1-ium-4-carboxylic Acid;chloride
2. Chebi:59790
3. 1-(3-cyano-3,3-diphenylpropyl)-4-phenylisonipecotic Acid Hydrochloride
4. 4-carboxy-1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidinium Chloride
5. 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylic Acid Hydrochloride
Molecular Weight | 461.0 g/mol |
---|---|
Molecular Formula | C28H29ClN2O2 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 7 |
Exact Mass | 460.1917559 g/mol |
Monoisotopic Mass | 460.1917559 g/mol |
Topological Polar Surface Area | 65.5 Ų |
Heavy Atom Count | 33 |
Formal Charge | 0 |
Complexity | 636 |
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 |
Related Excipient Companies
Excipients by Applications
ABOUT THIS PAGE
61
PharmaCompass offers a list of Difenoxin Hydrochloride 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 Difenoxin Hydrochloride manufacturer or Difenoxin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Difenoxin Hydrochloride manufacturer or Difenoxin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Difenoxin Hydrochloride API Price utilized in the formulation of products. Difenoxin Hydrochloride API Price is not always fixed or binding as the Difenoxin Hydrochloride Price is obtained through a variety of data sources. The Difenoxin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Difenoxin 1 mg/25ug AtSO4/du manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Difenoxin 1 mg/25ug AtSO4/du, including repackagers and relabelers. The FDA regulates Difenoxin 1 mg/25ug AtSO4/du manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Difenoxin 1 mg/25ug AtSO4/du 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 Difenoxin 1 mg/25ug AtSO4/du manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Difenoxin 1 mg/25ug AtSO4/du supplier is an individual or a company that provides Difenoxin 1 mg/25ug AtSO4/du active pharmaceutical ingredient (API) or Difenoxin 1 mg/25ug AtSO4/du finished formulations upon request. The Difenoxin 1 mg/25ug AtSO4/du suppliers may include Difenoxin 1 mg/25ug AtSO4/du API manufacturers, exporters, distributors and traders.
click here to find a list of Difenoxin 1 mg/25ug AtSO4/du suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Difenoxin 1 mg/25ug AtSO4/du DMF (Drug Master File) is a document detailing the whole manufacturing process of Difenoxin 1 mg/25ug AtSO4/du active pharmaceutical ingredient (API) in detail. Different forms of Difenoxin 1 mg/25ug AtSO4/du DMFs exist exist since differing nations have different regulations, such as Difenoxin 1 mg/25ug AtSO4/du USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Difenoxin 1 mg/25ug AtSO4/du DMF submitted to regulatory agencies in the US is known as a USDMF. Difenoxin 1 mg/25ug AtSO4/du USDMF includes data on Difenoxin 1 mg/25ug AtSO4/du's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Difenoxin 1 mg/25ug AtSO4/du USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Difenoxin 1 mg/25ug AtSO4/du suppliers with USDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Difenoxin 1 mg/25ug AtSO4/du as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Difenoxin 1 mg/25ug AtSO4/du API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Difenoxin 1 mg/25ug AtSO4/du as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Difenoxin 1 mg/25ug AtSO4/du and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Difenoxin 1 mg/25ug AtSO4/du NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Difenoxin 1 mg/25ug AtSO4/du suppliers with NDC on PharmaCompass.
Difenoxin 1 mg/25ug AtSO4/du 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 Difenoxin 1 mg/25ug AtSO4/du 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 Difenoxin 1 mg/25ug AtSO4/du GMP manufacturer or Difenoxin 1 mg/25ug AtSO4/du GMP API supplier for your needs.
A Difenoxin 1 mg/25ug AtSO4/du CoA (Certificate of Analysis) is a formal document that attests to Difenoxin 1 mg/25ug AtSO4/du's compliance with Difenoxin 1 mg/25ug AtSO4/du specifications and serves as a tool for batch-level quality control.
Difenoxin 1 mg/25ug AtSO4/du CoA mostly includes findings from lab analyses of a specific batch. For each Difenoxin 1 mg/25ug AtSO4/du 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.
Difenoxin 1 mg/25ug AtSO4/du may be tested according to a variety of international standards, such as European Pharmacopoeia (Difenoxin 1 mg/25ug AtSO4/du EP), Difenoxin 1 mg/25ug AtSO4/du JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Difenoxin 1 mg/25ug AtSO4/du USP).