Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
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
FDF
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
1. 6974-99-8
2. Nsc22053
3. 1h-indene,2,3-dihydro-2,4,7-trimethyl-
4. Dtxsid40281578
5. Zinc1589737
6. Nsc-22053
7. 1h-indene,3-dihydro-2,4,7-trimethyl-
8. Ds-002906
Molecular Weight | 160.25 g/mol |
---|---|
Molecular Formula | C12H16 |
XLogP3 | 3.7 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 0 |
Rotatable Bond Count | 0 |
Exact Mass | 160.125200510 g/mol |
Monoisotopic Mass | 160.125200510 g/mol |
Topological Polar Surface Area | 0 Ų |
Heavy Atom Count | 12 |
Formal Charge | 0 |
Complexity | 143 |
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 |
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Microcrystalline Cellulose API 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 Microcrystalline Cellulose API manufacturer or Microcrystalline Cellulose API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Microcrystalline Cellulose API manufacturer or Microcrystalline Cellulose API supplier.
PharmaCompass also assists you with knowing the Microcrystalline Cellulose API API Price utilized in the formulation of products. Microcrystalline Cellulose API API Price is not always fixed or binding as the Microcrystalline Cellulose API Price is obtained through a variety of data sources. The Microcrystalline Cellulose API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cellulose Microcrystalline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellulose Microcrystalline, including repackagers and relabelers. The FDA regulates Cellulose Microcrystalline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellulose Microcrystalline 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 Cellulose Microcrystalline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cellulose Microcrystalline supplier is an individual or a company that provides Cellulose Microcrystalline active pharmaceutical ingredient (API) or Cellulose Microcrystalline finished formulations upon request. The Cellulose Microcrystalline suppliers may include Cellulose Microcrystalline API manufacturers, exporters, distributors and traders.
click here to find a list of Cellulose Microcrystalline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cellulose Microcrystalline DMF (Drug Master File) is a document detailing the whole manufacturing process of Cellulose Microcrystalline active pharmaceutical ingredient (API) in detail. Different forms of Cellulose Microcrystalline DMFs exist exist since differing nations have different regulations, such as Cellulose Microcrystalline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cellulose Microcrystalline DMF submitted to regulatory agencies in the US is known as a USDMF. Cellulose Microcrystalline USDMF includes data on Cellulose Microcrystalline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cellulose Microcrystalline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cellulose Microcrystalline suppliers with USDMF on PharmaCompass.
Cellulose Microcrystalline 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 Cellulose Microcrystalline 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 Cellulose Microcrystalline GMP manufacturer or Cellulose Microcrystalline GMP API supplier for your needs.
A Cellulose Microcrystalline CoA (Certificate of Analysis) is a formal document that attests to Cellulose Microcrystalline's compliance with Cellulose Microcrystalline specifications and serves as a tool for batch-level quality control.
Cellulose Microcrystalline CoA mostly includes findings from lab analyses of a specific batch. For each Cellulose Microcrystalline 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.
Cellulose Microcrystalline may be tested according to a variety of international standards, such as European Pharmacopoeia (Cellulose Microcrystalline EP), Cellulose Microcrystalline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cellulose Microcrystalline USP).