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Looking for 3239-45-0 / Dexfenfluramine API manufacturers, exporters & distributors?

Dexfenfluramine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dexfenfluramine

Synonyms

3239-45-0, Isomeride, Adipomin, (+)-fenfluramine hydrochloride, Adifax, Redux

Cas Number

3239-45-0

Unique Ingredient Identifier (UNII)

PM28L0FHNP

About Dexfenfluramine

The S-isomer of FENFLURAMINE. It is a serotonin agonist and is used as an anorectic. Unlike fenfluramine, it does not possess any catecholamine agonist activity.

Dexfenfluramine Manufacturers

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

Dexfenfluramine Suppliers

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

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

Dexfenfluramine USDMF

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

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

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

Dexfenfluramine GMP

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

Dexfenfluramine CoA

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

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

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