Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
Drugs in Development
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]Related Excipient Companies
Solubilizers
Topical
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
ABOUT THIS PAGE
63
PharmaCompass offers a list of Collagenase Clostridium Histolyticum 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 Collagenase Clostridium Histolyticum manufacturer or Collagenase Clostridium Histolyticum supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Collagenase Clostridium Histolyticum manufacturer or Collagenase Clostridium Histolyticum supplier.
PharmaCompass also assists you with knowing the Collagenase Clostridium Histolyticum API Price utilized in the formulation of products. Collagenase Clostridium Histolyticum API Price is not always fixed or binding as the Collagenase Clostridium Histolyticum Price is obtained through a variety of data sources. The Collagenase Clostridium Histolyticum Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A XIAFLEX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XIAFLEX, including repackagers and relabelers. The FDA regulates XIAFLEX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XIAFLEX 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 XIAFLEX supplier is an individual or a company that provides XIAFLEX active pharmaceutical ingredient (API) or XIAFLEX finished formulations upon request. The XIAFLEX suppliers may include XIAFLEX API manufacturers, exporters, distributors and traders.
click here to find a list of XIAFLEX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 XIAFLEX as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for XIAFLEX 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 XIAFLEX 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 XIAFLEX and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a XIAFLEX NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of XIAFLEX suppliers with NDC on PharmaCompass.
XIAFLEX 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 XIAFLEX 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 XIAFLEX GMP manufacturer or XIAFLEX GMP API supplier for your needs.
A XIAFLEX CoA (Certificate of Analysis) is a formal document that attests to XIAFLEX's compliance with XIAFLEX specifications and serves as a tool for batch-level quality control.
XIAFLEX CoA mostly includes findings from lab analyses of a specific batch. For each XIAFLEX 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.
XIAFLEX may be tested according to a variety of international standards, such as European Pharmacopoeia (XIAFLEX EP), XIAFLEX JP (Japanese Pharmacopeia) and the US Pharmacopoeia (XIAFLEX USP).
