API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
USA (Orange Book)
0
Europe
Canada
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
87
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.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate, including repackagers and relabelers. The FDA regulates 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,3,5(10)-Estratriene-3,17beta-diol 3-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 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate supplier is an individual or a company that provides 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate active pharmaceutical ingredient (API) or 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate finished formulations upon request. The 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate suppliers may include 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate API manufacturers, exporters, distributors and traders.
click here to find a list of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate DMF (Drug Master File) is a document detailing the whole manufacturing process of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate active pharmaceutical ingredient (API) in detail. Different forms of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate DMFs exist exist since differing nations have different regulations, such as 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate DMF submitted to regulatory agencies in the US is known as a USDMF. 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate USDMF includes data on 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate suppliers with USDMF on PharmaCompass.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP of the European Pharmacopoeia monograph is often referred to as a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate Certificate of Suitability (COS). The purpose of a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate to their clients by showing that a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP has been issued for it. The manufacturer submits a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP holder for the record. Additionally, the data presented in the 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate DMF.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1,3,5(10)-Estratriene-3,17beta-diol 3-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 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate suppliers with CEP (COS) on PharmaCompass.
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 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate API and other APIs are published in this directory by the FDA.
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 1,3,5(10)-Estratriene-3,17beta-diol 3-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.
The NDC directory also contains data on finished compounded human drug products that contain 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate suppliers with NDC on PharmaCompass.
1,3,5(10)-Estratriene-3,17beta-diol 3-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 1,3,5(10)-Estratriene-3,17beta-diol 3-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 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate GMP manufacturer or 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate GMP API supplier for your needs.
A 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CoA (Certificate of Analysis) is a formal document that attests to 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate's compliance with 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate specifications and serves as a tool for batch-level quality control.
1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate CoA mostly includes findings from lab analyses of a specific batch. For each 1,3,5(10)-Estratriene-3,17beta-diol 3-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.
1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate may be tested according to a variety of international standards, such as European Pharmacopoeia (1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate EP), 1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,3,5(10)-Estratriene-3,17beta-diol 3-benzoate USP).