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Looking for 790704-50-6 / Oxaquin API manufacturers, exporters & distributors?

Oxaquin manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Oxaquin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Oxaquin manufacturer or Oxaquin supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxaquin manufacturer or Oxaquin supplier.

PharmaCompass also assists you with knowing the Oxaquin API Price utilized in the formulation of products. Oxaquin API Price is not always fixed or binding as the Oxaquin Price is obtained through a variety of data sources. The Oxaquin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Oxaquin

Synonyms

Mcb-3837, 1221r21zrq, Mcb 3837, 790704-50-6, 3-quinolinecarboxylic acid, 7-(4-((4-((5s)-5-((acetylamino)methyl)-2-oxo-3-oxazolidinyl)-2-fluorophenoxy)methyl)-4-(phosphonooxy)-1-piperidinyl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-, 7-(4-((4-((5s)-5-(acetamidomethyl)-2-oxo-oxazolidin-3-yl)-2-fluoro-phenoxy)methyl)-4-phosphonooxy-1-piperidyl)-1-cyclopropyl-6-fluoro-4-oxo-quinoline-3-carboxylic acid

Cas Number

790704-50-6

Unique Ingredient Identifier (UNII)

1221R21ZRQ

About Oxaquin

Quinolonyl-oxazolidinone Antibiotic DNV3837 is a prodrug of DNV3681, a small molecule quinolonyl-oxazolidinone antibiotic with activity against Gram-positive bacteria, including Clostridioides difficile. Upon intravenous administration, DNV3837 crosses the gastrointestinal barrier to reach the C. difficile infection site. The active drug DNV3681 may affect four bacterial targets including DNA-gyrase, topoisomerase IV, protein synthesis and aminoacyl-t-RNA synthetases, which leads to bacterial cell death. DNV3681 does not have antibacterial activity against aerobic and anaerobic Gram-negative bacteria, sparing intestinal Bacteroides spp. that provide colonization resistance in the digestive tract.

Oxaquin Manufacturers

A Oxaquin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxaquin, including repackagers and relabelers. The FDA regulates Oxaquin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxaquin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Oxaquin Suppliers

A Oxaquin supplier is an individual or a company that provides Oxaquin active pharmaceutical ingredient (API) or Oxaquin finished formulations upon request. The Oxaquin suppliers may include Oxaquin API manufacturers, exporters, distributors and traders.

Oxaquin GMP

Oxaquin 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 Oxaquin 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 Oxaquin GMP manufacturer or Oxaquin GMP API supplier for your needs.

Oxaquin CoA

A Oxaquin CoA (Certificate of Analysis) is a formal document that attests to Oxaquin's compliance with Oxaquin specifications and serves as a tool for batch-level quality control.

Oxaquin CoA mostly includes findings from lab analyses of a specific batch. For each Oxaquin 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.

Oxaquin may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxaquin EP), Oxaquin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxaquin USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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