Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
EDQM
0
USP
0
JP
0
Others
0
FDA Orange Book
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
China’s top API & intermediate manufacturer, delivering advanced CMO/CDMO solutions to 60+ countries, empowering global health progress
Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
INTERMEDIATE SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Dossiers
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Chewable Tablet
Dosage Strength : 11.3MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Chewable Tablet
Dosage Strength : 28.3MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Chewable Tablet
Dosage Strength : 68MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Chewable Tablet
Dosage Strength : 136MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
NEWS #PharmaBuzz
Global Sales Information
Market Place
ABOUT THIS PAGE
12
PharmaCompass offers a list of Afoxolaner API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Afoxolaner manufacturer or Afoxolaner supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Afoxolaner manufacturer or Afoxolaner supplier.
A Afoxolaner manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Afoxolaner, including repackagers and relabelers. The FDA regulates Afoxolaner manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Afoxolaner 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 Afoxolaner manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Afoxolaner supplier is an individual or a company that provides Afoxolaner active pharmaceutical ingredient (API) or Afoxolaner finished formulations upon request. The Afoxolaner suppliers may include Afoxolaner API manufacturers, exporters, distributors and traders.
click here to find a list of Afoxolaner suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information 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 Afoxolaner as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Afoxolaner 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 Afoxolaner 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 Afoxolaner and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Afoxolaner NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Afoxolaner suppliers with NDC on PharmaCompass.
Afoxolaner 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 Afoxolaner GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Afoxolaner GMP manufacturer or Afoxolaner GMP API supplier for your needs.
A Afoxolaner CoA (Certificate of Analysis) is a formal document that attests to Afoxolaner's compliance with Afoxolaner specifications and serves as a tool for batch-level quality control.
Afoxolaner CoA mostly includes findings from lab analyses of a specific batch. For each Afoxolaner 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.
Afoxolaner may be tested according to a variety of international standards, such as European Pharmacopoeia (Afoxolaner EP), Afoxolaner JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Afoxolaner USP).
