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PharmaCompass offers a list of Podophyllotoxin 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 Podophyllotoxin manufacturer or Podophyllotoxin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Podophyllotoxin manufacturer or Podophyllotoxin supplier.
PharmaCompass also assists you with knowing the Podophyllotoxin API Price utilized in the formulation of products. Podophyllotoxin API Price is not always fixed or binding as the Podophyllotoxin Price is obtained through a variety of data sources. The Podophyllotoxin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PODOFILOX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PODOFILOX, including repackagers and relabelers. The FDA regulates PODOFILOX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PODOFILOX 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 PODOFILOX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PODOFILOX supplier is an individual or a company that provides PODOFILOX active pharmaceutical ingredient (API) or PODOFILOX finished formulations upon request. The PODOFILOX suppliers may include PODOFILOX API manufacturers, exporters, distributors and traders.
click here to find a list of PODOFILOX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PODOFILOX DMF (Drug Master File) is a document detailing the whole manufacturing process of PODOFILOX active pharmaceutical ingredient (API) in detail. Different forms of PODOFILOX DMFs exist exist since differing nations have different regulations, such as PODOFILOX USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A PODOFILOX DMF submitted to regulatory agencies in the US is known as a USDMF. PODOFILOX USDMF includes data on PODOFILOX's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The PODOFILOX USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of PODOFILOX suppliers with USDMF on PharmaCompass.
A PODOFILOX written confirmation (PODOFILOX WC) is an official document issued by a regulatory agency to a PODOFILOX manufacturer, verifying that the manufacturing facility of a PODOFILOX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting PODOFILOX APIs or PODOFILOX finished pharmaceutical products to another nation, regulatory agencies frequently require a PODOFILOX WC (written confirmation) as part of the regulatory process.
click here to find a list of PODOFILOX suppliers with Written Confirmation (WC) 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 PODOFILOX as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PODOFILOX 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 PODOFILOX 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 PODOFILOX and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PODOFILOX NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PODOFILOX suppliers with NDC on PharmaCompass.
PODOFILOX 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 PODOFILOX 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 PODOFILOX GMP manufacturer or PODOFILOX GMP API supplier for your needs.
A PODOFILOX CoA (Certificate of Analysis) is a formal document that attests to PODOFILOX's compliance with PODOFILOX specifications and serves as a tool for batch-level quality control.
PODOFILOX CoA mostly includes findings from lab analyses of a specific batch. For each PODOFILOX 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.
PODOFILOX may be tested according to a variety of international standards, such as European Pharmacopoeia (PODOFILOX EP), PODOFILOX JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PODOFILOX USP).