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| Molecular Weight | 230.35 g/mol |
|---|---|
| Molecular Formula | CH7AlMgO10-4 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 0 |
| Exact Mass | 229.9705015 g/mol |
| Monoisotopic Mass | 229.9705015 g/mol |
| Topological Polar Surface Area | 70.2 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | -4 |
| Complexity | 22.9 |
| 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 | 10 |
ABOUT THIS PAGE
A Hydrotalcite Bp manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrotalcite Bp, including repackagers and relabelers. The FDA regulates Hydrotalcite Bp manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrotalcite Bp API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Hydrotalcite Bp supplier is an individual or a company that provides Hydrotalcite Bp active pharmaceutical ingredient (API) or Hydrotalcite Bp finished formulations upon request. The Hydrotalcite Bp suppliers may include Hydrotalcite Bp API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrotalcite Bp suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hydrotalcite Bp DMF (Drug Master File) is a document detailing the whole manufacturing process of Hydrotalcite Bp active pharmaceutical ingredient (API) in detail. Different forms of Hydrotalcite Bp DMFs exist exist since differing nations have different regulations, such as Hydrotalcite Bp USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hydrotalcite Bp DMF submitted to regulatory agencies in the US is known as a USDMF. Hydrotalcite Bp USDMF includes data on Hydrotalcite Bp's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hydrotalcite Bp USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hydrotalcite Bp suppliers with USDMF on PharmaCompass.
A Hydrotalcite Bp written confirmation (Hydrotalcite Bp WC) is an official document issued by a regulatory agency to a Hydrotalcite Bp manufacturer, verifying that the manufacturing facility of a Hydrotalcite Bp active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hydrotalcite Bp APIs or Hydrotalcite Bp finished pharmaceutical products to another nation, regulatory agencies frequently require a Hydrotalcite Bp WC (written confirmation) as part of the regulatory process.
click here to find a list of Hydrotalcite Bp suppliers with Written Confirmation (WC) on PharmaCompass.
Hydrotalcite Bp 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 Hydrotalcite Bp 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 Hydrotalcite Bp GMP manufacturer or Hydrotalcite Bp GMP API supplier for your needs.
A Hydrotalcite Bp CoA (Certificate of Analysis) is a formal document that attests to Hydrotalcite Bp's compliance with Hydrotalcite Bp specifications and serves as a tool for batch-level quality control.
Hydrotalcite Bp CoA mostly includes findings from lab analyses of a specific batch. For each Hydrotalcite Bp 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.
Hydrotalcite Bp may be tested according to a variety of international standards, such as European Pharmacopoeia (Hydrotalcite Bp EP), Hydrotalcite Bp JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hydrotalcite Bp USP).
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