API Suppliers
0
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
EU WC
0
Listed Suppliers
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
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
20
PharmaCompass offers a list of Phoxim 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 Phoxim manufacturer or Phoxim supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phoxim manufacturer or Phoxim supplier.
PharmaCompass also assists you with knowing the Phoxim API Price utilized in the formulation of products. Phoxim API Price is not always fixed or binding as the Phoxim Price is obtained through a variety of data sources. The Phoxim Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Phoxim manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phoxim, including repackagers and relabelers. The FDA regulates Phoxim manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phoxim 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 Phoxim supplier is an individual or a company that provides Phoxim active pharmaceutical ingredient (API) or Phoxim finished formulations upon request. The Phoxim suppliers may include Phoxim API manufacturers, exporters, distributors and traders.
Phoxim 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 Phoxim 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 Phoxim GMP manufacturer or Phoxim GMP API supplier for your needs.
A Phoxim CoA (Certificate of Analysis) is a formal document that attests to Phoxim's compliance with Phoxim specifications and serves as a tool for batch-level quality control.
Phoxim CoA mostly includes findings from lab analyses of a specific batch. For each Phoxim 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.
Phoxim may be tested according to a variety of international standards, such as European Pharmacopoeia (Phoxim EP), Phoxim JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phoxim USP).