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Looking for 73-34-7 / Rhamnose API manufacturers, exporters & distributors?

Rhamnose manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Rhamnose 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 Rhamnose manufacturer or Rhamnose supplier for your needs.

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

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

API | Excipient name

Rhamnose

Synonyms

3615-41-6, Aldehydo-l-rhamnose, L-mannomethylose, Isodulcitol, Rhamnose, l-, Locaose

Cas Number

73-34-7

Unique Ingredient Identifier (UNII)

QN34XC755A

About Rhamnose

A methylpentose whose L- isomer is found naturally in many plant glycosides and some gram-negative bacterial lipopolysaccharides.

Rhamnose Manufacturers

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

click here to find a list of Rhamnose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Rhamnose Suppliers

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

click here to find a list of Rhamnose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Rhamnose USDMF

A Rhamnose DMF (Drug Master File) is a document detailing the whole manufacturing process of Rhamnose active pharmaceutical ingredient (API) in detail. Different forms of Rhamnose DMFs exist exist since differing nations have different regulations, such as Rhamnose USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Rhamnose DMF submitted to regulatory agencies in the US is known as a USDMF. Rhamnose USDMF includes data on Rhamnose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rhamnose USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Rhamnose suppliers with USDMF on PharmaCompass.

Rhamnose GMP

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

Rhamnose CoA

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

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

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