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1. Jn7w3m3oi7
2. Vitamin A Acetate C20-d3
| Molecular Weight | 331.5 g/mol |
|---|---|
| Molecular Formula | C22H32O2 |
| XLogP3 | 6.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 7 |
| Exact Mass | 331.259060497 g/mol |
| Monoisotopic Mass | 331.259060497 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 596 |
| Isotope Atom Count | 3 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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A Gildeuretinol Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gildeuretinol Acetate, including repackagers and relabelers. The FDA regulates Gildeuretinol Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gildeuretinol Acetate 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 Gildeuretinol Acetate supplier is an individual or a company that provides Gildeuretinol Acetate active pharmaceutical ingredient (API) or Gildeuretinol Acetate finished formulations upon request. The Gildeuretinol Acetate suppliers may include Gildeuretinol Acetate API manufacturers, exporters, distributors and traders.
Gildeuretinol Acetate 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 Gildeuretinol Acetate 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 Gildeuretinol Acetate GMP manufacturer or Gildeuretinol Acetate GMP API supplier for your needs.
A Gildeuretinol Acetate CoA (Certificate of Analysis) is a formal document that attests to Gildeuretinol Acetate's compliance with Gildeuretinol Acetate specifications and serves as a tool for batch-level quality control.
Gildeuretinol Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Gildeuretinol Acetate 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.
Gildeuretinol Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Gildeuretinol Acetate EP), Gildeuretinol Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gildeuretinol Acetate USP).
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