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Looking for 765922-62-1 / Flutemetamol API manufacturers, exporters & distributors?

Flutemetamol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Flutemetamol

Synonyms

Flutemetamol f 18, Vizamyl, Flutemetamol (18f), 18f-flutemetamol, Flutemetamol f18, Flutemetamol ((sup18)f)

Cas Number

765922-62-1

Unique Ingredient Identifier (UNII)

L49M066S0O

About Flutemetamol

Flutemetamol F 18 is a radiopharmaceutical containing flutemetamol, a thioflavin derivative of Pittsburgh compound B (PiB) labeled with the radioisotope fluorine F18 that can be used to detect beta-amyloid deposition upon positron emission tomography (PET). After intravenous administration of flutemetamol F 18, the flutemetamol moiety selectively accumulates in and binds to cerebral fibrillar amyloid-beta in the brain. The fluorine F18 radioisotope moiety is detected using PET, which allows imaging and quantification of amyloid-beta density. Amyloid plaque deposition is linked to cognitive decline, including Alzheimer's disease, and may be linked to chemotherapy-induced cognitive impairment (CICI).

Flutemetamol Manufacturers

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

Flutemetamol Suppliers

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

Flutemetamol GMP

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

Flutemetamol CoA

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

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

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