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Looking for 153-18-4 / Rutin API manufacturers, exporters & distributors?

Rutin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Rutin

Synonyms

153-18-4, Rutoside, Quercetin 3-rutinoside, Birutan, Phytomelin, Myrticolorin

Cas Number

153-18-4

Unique Ingredient Identifier (UNII)

5G06TVY3R7

About Rutin

A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.

1416-01-9 Manufacturers

A 1416-01-9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1416-01-9, including repackagers and relabelers. The FDA regulates 1416-01-9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1416-01-9 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 1416-01-9 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

1416-01-9 Suppliers

A 1416-01-9 supplier is an individual or a company that provides 1416-01-9 active pharmaceutical ingredient (API) or 1416-01-9 finished formulations upon request. The 1416-01-9 suppliers may include 1416-01-9 API manufacturers, exporters, distributors and traders.

click here to find a list of 1416-01-9 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

1416-01-9 USDMF

A 1416-01-9 DMF (Drug Master File) is a document detailing the whole manufacturing process of 1416-01-9 active pharmaceutical ingredient (API) in detail. Different forms of 1416-01-9 DMFs exist exist since differing nations have different regulations, such as 1416-01-9 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 1416-01-9 DMF submitted to regulatory agencies in the US is known as a USDMF. 1416-01-9 USDMF includes data on 1416-01-9's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1416-01-9 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 1416-01-9 suppliers with USDMF on PharmaCompass.

1416-01-9 CEP

A 1416-01-9 CEP of the European Pharmacopoeia monograph is often referred to as a 1416-01-9 Certificate of Suitability (COS). The purpose of a 1416-01-9 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1416-01-9 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1416-01-9 to their clients by showing that a 1416-01-9 CEP has been issued for it. The manufacturer submits a 1416-01-9 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1416-01-9 CEP holder for the record. Additionally, the data presented in the 1416-01-9 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1416-01-9 DMF.

A 1416-01-9 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1416-01-9 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of 1416-01-9 suppliers with CEP (COS) on PharmaCompass.

1416-01-9 WC

A 1416-01-9 written confirmation (1416-01-9 WC) is an official document issued by a regulatory agency to a 1416-01-9 manufacturer, verifying that the manufacturing facility of a 1416-01-9 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1416-01-9 APIs or 1416-01-9 finished pharmaceutical products to another nation, regulatory agencies frequently require a 1416-01-9 WC (written confirmation) as part of the regulatory process.

click here to find a list of 1416-01-9 suppliers with Written Confirmation (WC) on PharmaCompass.

1416-01-9 GMP

1416-01-9 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 1416-01-9 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 1416-01-9 GMP manufacturer or 1416-01-9 GMP API supplier for your needs.

1416-01-9 CoA

A 1416-01-9 CoA (Certificate of Analysis) is a formal document that attests to 1416-01-9's compliance with 1416-01-9 specifications and serves as a tool for batch-level quality control.

1416-01-9 CoA mostly includes findings from lab analyses of a specific batch. For each 1416-01-9 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.

1416-01-9 may be tested according to a variety of international standards, such as European Pharmacopoeia (1416-01-9 EP), 1416-01-9 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1416-01-9 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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