Synopsis
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| Molecular Weight | 902.9 g/mol |
|---|---|
| Molecular Formula | C39H66O23 |
| XLogP3 | -3.9 |
| Hydrogen Bond Donor Count | 11 |
| Hydrogen Bond Acceptor Count | 23 |
| Rotatable Bond Count | 23 |
| Exact Mass | 902.39948835 g/mol |
| Monoisotopic Mass | 902.39948835 g/mol |
| Topological Polar Surface Area | 349 Ų |
| Heavy Atom Count | 62 |
| Formal Charge | 0 |
| Complexity | 1380 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 21 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
A SODIUM STARCH GLYOLATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM STARCH GLYOLATE, including repackagers and relabelers. The FDA regulates SODIUM STARCH GLYOLATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM STARCH GLYOLATE 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 SODIUM STARCH GLYOLATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SODIUM STARCH GLYOLATE supplier is an individual or a company that provides SODIUM STARCH GLYOLATE active pharmaceutical ingredient (API) or SODIUM STARCH GLYOLATE finished formulations upon request. The SODIUM STARCH GLYOLATE suppliers may include SODIUM STARCH GLYOLATE API manufacturers, exporters, distributors and traders.
click here to find a list of SODIUM STARCH GLYOLATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SODIUM STARCH GLYOLATE DMF (Drug Master File) is a document detailing the whole manufacturing process of SODIUM STARCH GLYOLATE active pharmaceutical ingredient (API) in detail. Different forms of SODIUM STARCH GLYOLATE DMFs exist exist since differing nations have different regulations, such as SODIUM STARCH GLYOLATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A SODIUM STARCH GLYOLATE DMF submitted to regulatory agencies in the US is known as a USDMF. SODIUM STARCH GLYOLATE USDMF includes data on SODIUM STARCH GLYOLATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The SODIUM STARCH GLYOLATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of SODIUM STARCH GLYOLATE suppliers with USDMF on PharmaCompass.
SODIUM STARCH GLYOLATE 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 SODIUM STARCH GLYOLATE 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 SODIUM STARCH GLYOLATE GMP manufacturer or SODIUM STARCH GLYOLATE GMP API supplier for your needs.
A SODIUM STARCH GLYOLATE CoA (Certificate of Analysis) is a formal document that attests to SODIUM STARCH GLYOLATE's compliance with SODIUM STARCH GLYOLATE specifications and serves as a tool for batch-level quality control.
SODIUM STARCH GLYOLATE CoA mostly includes findings from lab analyses of a specific batch. For each SODIUM STARCH GLYOLATE 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.
SODIUM STARCH GLYOLATE may be tested according to a variety of international standards, such as European Pharmacopoeia (SODIUM STARCH GLYOLATE EP), SODIUM STARCH GLYOLATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SODIUM STARCH GLYOLATE USP).
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