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Looking for 5578-73-4 / Sanguinarine API manufacturers, exporters & distributors?

Sanguinarine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sanguinarine

Synonyms

Sanguinarine chloride, 5578-73-4, Viadent, Sanguinarine chloride hydrate, Sanguinarine hydrochloride, Sanguinarine (chloride)

Cas Number

5578-73-4

Unique Ingredient Identifier (UNII)

B8Z8J4400H

Sanguinarine Manufacturers

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

Sanguinarine Suppliers

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

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

Sanguinarine USDMF

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

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

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

Sanguinarine GMP

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

Sanguinarine CoA

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

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

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