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Looking for 489-84-9 / Guaiazulene API manufacturers, exporters & distributors?

Guaiazulene manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Guaiazulene

Synonyms

489-84-9, 1,4-dimethyl-7-isopropylazulene, Vetivazulen, 7-isopropyl-1,4-dimethylazulene, Azulon, Kessazulen

Cas Number

489-84-9

Unique Ingredient Identifier (UNII)

2OZ1K9JKQC

About Guaiazulene

azulon is a natural product found in Mikania cordifolia, Santolina corsica, and other organisms with data available.

Guaiazulene Manufacturers

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

Guaiazulene Suppliers

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

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

Guaiazulene WC

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

click here to find a list of Guaiazulene suppliers with Written Confirmation (WC) on PharmaCompass.

Guaiazulene GMP

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

Guaiazulene CoA

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

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

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