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1. Cobalt;chloride
2. 34240-80-7
Molecular Weight | 94.38 g/mol |
---|---|
Molecular Formula | ClCo- |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 0 |
Exact Mass | 93.902046 g/mol |
Monoisotopic Mass | 93.902046 g/mol |
Topological Polar Surface Area | 0 Ų |
Heavy Atom Count | 2 |
Formal Charge | -1 |
Complexity | 0 |
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 | 2 |
Regulatory Info :
Registration Country :
Iron; Cupric Chloride; Cobalt; chloride; Pyridoxine; Vitamin B 12; Vitamin- B12
Brand Name : Feradit
Dosage Form :
Dosage Strength :
Packaging : 100 ML Vial
Approval Date :
Application Number :
Regulatory Info :
Registration Country :
Regulatory Info :
Registration Country :
Iron; Cupric Chloride; Cobalt; chloride; Pyridoxine; Vitamin B 12; Vitamin- B12
Brand Name : Feradit
Dosage Form :
Dosage Strength :
Packaging : 100 ML Vial
Approval Date :
Application Number :
Regulatory Info :
Registration Country :
Packaging : 100 ML Vial
Regulatory Info :
Iron; Cupric Chloride; Cobalt; chloride; Pyridoxine; Vitamin B 12; Vitamin- B12
Dosage :
Dosage Strength :
Brand Name : Feradit
Approval Date :
Application Number :
Registration Country :
ABOUT THIS PAGE
A Cobalt;Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cobalt;Chloride, including repackagers and relabelers. The FDA regulates Cobalt;Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cobalt;Chloride 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 Cobalt;Chloride supplier is an individual or a company that provides Cobalt;Chloride active pharmaceutical ingredient (API) or Cobalt;Chloride finished formulations upon request. The Cobalt;Chloride suppliers may include Cobalt;Chloride API manufacturers, exporters, distributors and traders.
Cobalt;Chloride 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 Cobalt;Chloride 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 Cobalt;Chloride GMP manufacturer or Cobalt;Chloride GMP API supplier for your needs.
A Cobalt;Chloride CoA (Certificate of Analysis) is a formal document that attests to Cobalt;Chloride's compliance with Cobalt;Chloride specifications and serves as a tool for batch-level quality control.
Cobalt;Chloride CoA mostly includes findings from lab analyses of a specific batch. For each Cobalt;Chloride 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.
Cobalt;Chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Cobalt;Chloride EP), Cobalt;Chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cobalt;Chloride USP).
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