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| Molecular Weight | 380.4 g/mol |
|---|---|
| Molecular Formula | C18H24N2O7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 380.15835111 g/mol |
| Monoisotopic Mass | 380.15835111 g/mol |
| Topological Polar Surface Area | 122 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 472 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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USDMF
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A Methscopolamine Nitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methscopolamine Nitrate, including repackagers and relabelers. The FDA regulates Methscopolamine Nitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methscopolamine Nitrate 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 Methscopolamine Nitrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methscopolamine Nitrate supplier is an individual or a company that provides Methscopolamine Nitrate active pharmaceutical ingredient (API) or Methscopolamine Nitrate finished formulations upon request. The Methscopolamine Nitrate suppliers may include Methscopolamine Nitrate API manufacturers, exporters, distributors and traders.
click here to find a list of Methscopolamine Nitrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methscopolamine Nitrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Methscopolamine Nitrate active pharmaceutical ingredient (API) in detail. Different forms of Methscopolamine Nitrate DMFs exist exist since differing nations have different regulations, such as Methscopolamine Nitrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methscopolamine Nitrate DMF submitted to regulatory agencies in the US is known as a USDMF. Methscopolamine Nitrate USDMF includes data on Methscopolamine Nitrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methscopolamine Nitrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Methscopolamine Nitrate suppliers with USDMF on PharmaCompass.
Methscopolamine Nitrate 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 Methscopolamine Nitrate 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 Methscopolamine Nitrate GMP manufacturer or Methscopolamine Nitrate GMP API supplier for your needs.
A Methscopolamine Nitrate CoA (Certificate of Analysis) is a formal document that attests to Methscopolamine Nitrate's compliance with Methscopolamine Nitrate specifications and serves as a tool for batch-level quality control.
Methscopolamine Nitrate CoA mostly includes findings from lab analyses of a specific batch. For each Methscopolamine Nitrate 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.
Methscopolamine Nitrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Methscopolamine Nitrate EP), Methscopolamine Nitrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methscopolamine Nitrate USP).
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