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1. Quinidex (tn)
2. Quinidine Sulfate (usp)
3. Dtxsid80975964
4. Quinidine Sulfate Hydrate (jp17)
5. Akos015895974
6. D02272
7. Sulfuric Acid--6'-methoxycinchonan-9-ol--water (1/2/2)
8. (s)-[(2r,5r)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;sulfuric Acid;dihydrate
9. 60553-86-8
Molecular Weight | 782.9 g/mol |
---|---|
Molecular Formula | C40H54N4O10S |
Hydrogen Bond Donor Count | 6 |
Hydrogen Bond Acceptor Count | 14 |
Rotatable Bond Count | 8 |
Exact Mass | 782.35606511 g/mol |
Monoisotopic Mass | 782.35606511 g/mol |
Topological Polar Surface Area | 176 Ų |
Heavy Atom Count | 55 |
Formal Charge | 0 |
Complexity | 538 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 5 |
1 of 2 | |
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Drug Name | Quinidine sulfate |
Drug Label | Quinidine is an antimalarial schizonticide and an antiarrhythmic agent with class 1A activity; it is the -isomer of quinine, and its molecular weight is 324.43. dQuinidine sulfate is the sulfate salt of quinidine; its chemical name is cinchonan-9-ol,... |
Active Ingredient | Quinidine sulfate |
Dosage Form | Tablet, extended release; Tablet |
Route | Oral |
Strength | 200mg; 300mg |
Market Status | Prescription |
Company | Sandoz; Watson Labs; Teva Pharms; Mutual Pharm |
2 of 2 | |
---|---|
Drug Name | Quinidine sulfate |
Drug Label | Quinidine is an antimalarial schizonticide and an antiarrhythmic agent with class 1A activity; it is the -isomer of quinine, and its molecular weight is 324.43. dQuinidine sulfate is the sulfate salt of quinidine; its chemical name is cinchonan-9-ol,... |
Active Ingredient | Quinidine sulfate |
Dosage Form | Tablet, extended release; Tablet |
Route | Oral |
Strength | 200mg; 300mg |
Market Status | Prescription |
Company | Sandoz; Watson Labs; Teva Pharms; Mutual Pharm |
ABOUT THIS PAGE
A Quinidine Sulfate Hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinidine Sulfate Hydrate, including repackagers and relabelers. The FDA regulates Quinidine Sulfate Hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinidine Sulfate Hydrate 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 Quinidine Sulfate Hydrate supplier is an individual or a company that provides Quinidine Sulfate Hydrate active pharmaceutical ingredient (API) or Quinidine Sulfate Hydrate finished formulations upon request. The Quinidine Sulfate Hydrate suppliers may include Quinidine Sulfate Hydrate API manufacturers, exporters, distributors and traders.
Quinidine Sulfate Hydrate 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 Quinidine Sulfate Hydrate 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 Quinidine Sulfate Hydrate GMP manufacturer or Quinidine Sulfate Hydrate GMP API supplier for your needs.
A Quinidine Sulfate Hydrate CoA (Certificate of Analysis) is a formal document that attests to Quinidine Sulfate Hydrate's compliance with Quinidine Sulfate Hydrate specifications and serves as a tool for batch-level quality control.
Quinidine Sulfate Hydrate CoA mostly includes findings from lab analyses of a specific batch. For each Quinidine Sulfate Hydrate 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.
Quinidine Sulfate Hydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Quinidine Sulfate Hydrate EP), Quinidine Sulfate Hydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Quinidine Sulfate Hydrate USP).
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