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1. D-amphetamine Adipate
2. Yyi1a8w4tq
3. 64770-52-1
4. Unii-yyi1a8w4tq
5. Chembl1200782
6. Schembl11760798
7. Dtxsid90215080
8. Dextroamphetamine Adipate [vandf]
9. Dextroamphetamine Adipate [orange Book]
10. Delcobese Component Dextroamphetamine Adipate
11. Dextroamphetamine Adipate Component Of Delcobese
12. Q27294789
13. Benzeneethanamine, .alpha.-methyl-, (s)-, Hexanedioate (1:1)
14. Hexanedioic Acid, Compd. With (.alpha.s)-.alpha.-methylbenzeneethanamine (1:1)
| Molecular Weight | 281.35 g/mol |
|---|---|
| Molecular Formula | C15H23NO4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 281.16270821 g/mol |
| Monoisotopic Mass | 281.16270821 g/mol |
| Topological Polar Surface Area | 101 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 198 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
A Dextroamphetamine Adipate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextroamphetamine Adipate, including repackagers and relabelers. The FDA regulates Dextroamphetamine Adipate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextroamphetamine Adipate 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 Dextroamphetamine Adipate supplier is an individual or a company that provides Dextroamphetamine Adipate active pharmaceutical ingredient (API) or Dextroamphetamine Adipate finished formulations upon request. The Dextroamphetamine Adipate suppliers may include Dextroamphetamine Adipate API manufacturers, exporters, distributors and traders.
Dextroamphetamine Adipate 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 Dextroamphetamine Adipate 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 Dextroamphetamine Adipate GMP manufacturer or Dextroamphetamine Adipate GMP API supplier for your needs.
A Dextroamphetamine Adipate CoA (Certificate of Analysis) is a formal document that attests to Dextroamphetamine Adipate's compliance with Dextroamphetamine Adipate specifications and serves as a tool for batch-level quality control.
Dextroamphetamine Adipate CoA mostly includes findings from lab analyses of a specific batch. For each Dextroamphetamine Adipate 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.
Dextroamphetamine Adipate may be tested according to a variety of international standards, such as European Pharmacopoeia (Dextroamphetamine Adipate EP), Dextroamphetamine Adipate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dextroamphetamine Adipate USP).
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