API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
Other Certificates
0
Other 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
53
PharmaCompass offers a list of Phenothrin 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 Phenothrin manufacturer or Phenothrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenothrin manufacturer or Phenothrin supplier.
PharmaCompass also assists you with knowing the Phenothrin API Price utilized in the formulation of products. Phenothrin API Price is not always fixed or binding as the Phenothrin Price is obtained through a variety of data sources. The Phenothrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Phenothrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phenothrin, including repackagers and relabelers. The FDA regulates Phenothrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phenothrin 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 Phenothrin supplier is an individual or a company that provides Phenothrin active pharmaceutical ingredient (API) or Phenothrin finished formulations upon request. The Phenothrin suppliers may include Phenothrin API manufacturers, exporters, distributors and traders.
click here to find a list of Phenothrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Phenothrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Phenothrin active pharmaceutical ingredient (API) in detail. Different forms of Phenothrin DMFs exist exist since differing nations have different regulations, such as Phenothrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Phenothrin DMF submitted to regulatory agencies in the US is known as a USDMF. Phenothrin USDMF includes data on Phenothrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Phenothrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Phenothrin suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Phenothrin Drug Master File in Japan (Phenothrin JDMF) empowers Phenothrin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Phenothrin JDMF during the approval evaluation for pharmaceutical products. At the time of Phenothrin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Phenothrin suppliers with JDMF on PharmaCompass.
Phenothrin 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 Phenothrin 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 Phenothrin GMP manufacturer or Phenothrin GMP API supplier for your needs.
A Phenothrin CoA (Certificate of Analysis) is a formal document that attests to Phenothrin's compliance with Phenothrin specifications and serves as a tool for batch-level quality control.
Phenothrin CoA mostly includes findings from lab analyses of a specific batch. For each Phenothrin 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.
Phenothrin may be tested according to a variety of international standards, such as European Pharmacopoeia (Phenothrin EP), Phenothrin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Phenothrin USP).