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1. Amdinocillin Pivoxil
2. Fl 1039
3. Fl-1039
4. Fl1039
5. Hydrochloride, Pivmecillinam
6. Mecillinam Pivaloyl Ester
7. Pivaloyl Ester, Mecillinam
8. Pivamdinocillin
9. Pivmecillinam
10. Pivmecillinam Hydrochloride
11. Pivoxil, Amdinocillin
1. Pivmecilinamo Clorhidrato
2. Chebi:51213
3. Schembl1650614
4. [(2,2-dimethylpropanoyl)oxy]methyl 6beta-[(azepan-1-ylmethylidene)amino]-2,2-dimethylpenam-3alpha-carboxylate Hydrochloride
5. 2,2-dimethylpropanoyloxymethyl (2s,5r,6r)-6-(azepan-1-ylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate;hydron;chloride
| Molecular Weight | 476.0 g/mol |
|---|---|
| Molecular Formula | C21H34ClN3O5S |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 8 |
| Exact Mass | 475.1907701 g/mol |
| Monoisotopic Mass | 475.1907701 g/mol |
| Topological Polar Surface Area | 114 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 710 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
Anti-Infective Agents, Urinary
Substances capable of killing agents causing urinary tract infections or of preventing them from spreading. (See all compounds classified as Anti-Infective Agents, Urinary.)
ABOUT THIS PAGE
A Pivmecilinamo Clorhidrato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pivmecilinamo Clorhidrato, including repackagers and relabelers. The FDA regulates Pivmecilinamo Clorhidrato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pivmecilinamo Clorhidrato 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 Pivmecilinamo Clorhidrato supplier is an individual or a company that provides Pivmecilinamo Clorhidrato active pharmaceutical ingredient (API) or Pivmecilinamo Clorhidrato finished formulations upon request. The Pivmecilinamo Clorhidrato suppliers may include Pivmecilinamo Clorhidrato API manufacturers, exporters, distributors and traders.
click here to find a list of Pivmecilinamo Clorhidrato suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pivmecilinamo Clorhidrato DMF (Drug Master File) is a document detailing the whole manufacturing process of Pivmecilinamo Clorhidrato active pharmaceutical ingredient (API) in detail. Different forms of Pivmecilinamo Clorhidrato DMFs exist exist since differing nations have different regulations, such as Pivmecilinamo Clorhidrato USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pivmecilinamo Clorhidrato DMF submitted to regulatory agencies in the US is known as a USDMF. Pivmecilinamo Clorhidrato USDMF includes data on Pivmecilinamo Clorhidrato's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pivmecilinamo Clorhidrato USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pivmecilinamo Clorhidrato suppliers with USDMF on PharmaCompass.
Pivmecilinamo Clorhidrato 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 Pivmecilinamo Clorhidrato 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 Pivmecilinamo Clorhidrato GMP manufacturer or Pivmecilinamo Clorhidrato GMP API supplier for your needs.
A Pivmecilinamo Clorhidrato CoA (Certificate of Analysis) is a formal document that attests to Pivmecilinamo Clorhidrato's compliance with Pivmecilinamo Clorhidrato specifications and serves as a tool for batch-level quality control.
Pivmecilinamo Clorhidrato CoA mostly includes findings from lab analyses of a specific batch. For each Pivmecilinamo Clorhidrato 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.
Pivmecilinamo Clorhidrato may be tested according to a variety of international standards, such as European Pharmacopoeia (Pivmecilinamo Clorhidrato EP), Pivmecilinamo Clorhidrato JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pivmecilinamo Clorhidrato USP).
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