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Looking for 50-50-0 / Estradiol Benzoate API manufacturers, exporters & distributors?

Estradiol Benzoate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Estradiol Benzoate

Synonyms

50-50-0, Benzhormovarine, Benzoestrofol, Benovocylin, Estradiol 3-benzoate, Oestradiol benzoate

Cas Number

50-50-0

Unique Ingredient Identifier (UNII)

1S4CJB5ZGN

About Estradiol Benzoate

Estradiol Benzoate is the synthetic benzoate ester of estradiol, a steroid sex hormone vital to the maintenance of fertility and secondary sexual characteristics in females. As the primary, most potent estrogen hormone produced by the ovaries, estradiol binds to and activates specific nuclear receptors. This agent exhibits mild anabolic and metabolic properties, and increases blood coagulability. (NCI04)

Estradiol Benzoate Manufacturers

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

Estradiol Benzoate Suppliers

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

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

Estradiol Benzoate USDMF

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

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

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

Estradiol Benzoate CEP

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

A Estradiol Benzoate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Estradiol Benzoate 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 Estradiol Benzoate suppliers with CEP (COS) on PharmaCompass.

Estradiol Benzoate NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Estradiol Benzoate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Estradiol Benzoate API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Estradiol Benzoate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Estradiol Benzoate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Estradiol Benzoate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Estradiol Benzoate suppliers with NDC on PharmaCompass.

Estradiol Benzoate GMP

Estradiol Benzoate 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 Estradiol Benzoate 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 Estradiol Benzoate GMP manufacturer or Estradiol Benzoate GMP API supplier for your needs.

Estradiol Benzoate CoA

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

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

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