X
API Suppliers
0
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
50
PharmaCompass offers a list of Enobosarm 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 Enobosarm manufacturer or Enobosarm supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Enobosarm manufacturer or Enobosarm supplier.
PharmaCompass also assists you with knowing the Enobosarm API Price utilized in the formulation of products. Enobosarm API Price is not always fixed or binding as the Enobosarm Price is obtained through a variety of data sources. The Enobosarm Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Enobosarm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enobosarm, including repackagers and relabelers. The FDA regulates Enobosarm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enobosarm API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Enobosarm supplier is an individual or a company that provides Enobosarm active pharmaceutical ingredient (API) or Enobosarm finished formulations upon request. The Enobosarm suppliers may include Enobosarm API manufacturers, exporters, distributors and traders.
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 Enobosarm as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Enobosarm 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 Enobosarm 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 Enobosarm and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Enobosarm NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Enobosarm suppliers with NDC on PharmaCompass.
Enobosarm 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 Enobosarm 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 Enobosarm GMP manufacturer or Enobosarm GMP API supplier for your needs.
A Enobosarm CoA (Certificate of Analysis) is a formal document that attests to Enobosarm's compliance with Enobosarm specifications and serves as a tool for batch-level quality control.
Enobosarm CoA mostly includes findings from lab analyses of a specific batch. For each Enobosarm 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.
Enobosarm may be tested according to a variety of international standards, such as European Pharmacopoeia (Enobosarm EP), Enobosarm JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Enobosarm USP).
Market Place
