Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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VMF
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EDQM
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USP
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JP
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Others
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FDA Orange Book
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Europe
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
API SUPPLIERS
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Jai Radhe Sales is your partner for all your sourcing needs.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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NDC API
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Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
About the Company : Synnat Pharma is a fast-growing pharmaceutical company focused on the development, identification, production, and distribution of phytochemicals and botanical extracts. Its APIs a...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales, founded in 1999, is a global distributor specializing in high-quality pharmaceutical ingredients from India. It offers complete sourcing solutions, technical and r...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
About the Company : Willow Birch Pharma, Inc. is a premier supplier of bulk APIs to North American Compounding Pharmacies, sourcing from FDA registered and GMP manufacturers. With licenses in all 50 s...
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API Imports and Exports
FDF Dossiers
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Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Thickeners and Stabilizers
Coating Systems & Additives
Taste Masking
Chewable & Orodispersible Aids
Parenteral
Granulation
Direct Compression
Controlled & Modified Release
Co-Processed Excipients
Fillers, Diluents & Binders
Market Place
FDF DOSSIERS
Reply
15 Jul 2022
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ABOUT THIS PAGE
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PharmaCompass offers a list of Podophyllum Resin 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 Podophyllum Resin manufacturer or Podophyllum Resin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Podophyllum Resin manufacturer or Podophyllum Resin supplier.
PharmaCompass also assists you with knowing the Podophyllum Resin API Price utilized in the formulation of products. Podophyllum Resin API Price is not always fixed or binding as the Podophyllum Resin Price is obtained through a variety of data sources. The Podophyllum Resin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Resin, Podophyllum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resin, Podophyllum, including repackagers and relabelers. The FDA regulates Resin, Podophyllum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resin, Podophyllum 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 Resin, Podophyllum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Resin, Podophyllum supplier is an individual or a company that provides Resin, Podophyllum active pharmaceutical ingredient (API) or Resin, Podophyllum finished formulations upon request. The Resin, Podophyllum suppliers may include Resin, Podophyllum API manufacturers, exporters, distributors and traders.
click here to find a list of Resin, Podophyllum 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 Resin, Podophyllum as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Resin, Podophyllum 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 Resin, Podophyllum 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 Resin, Podophyllum and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Resin, Podophyllum NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Resin, Podophyllum suppliers with NDC on PharmaCompass.
Resin, Podophyllum 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 Resin, Podophyllum 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 Resin, Podophyllum GMP manufacturer or Resin, Podophyllum GMP API supplier for your needs.
A Resin, Podophyllum CoA (Certificate of Analysis) is a formal document that attests to Resin, Podophyllum's compliance with Resin, Podophyllum specifications and serves as a tool for batch-level quality control.
Resin, Podophyllum CoA mostly includes findings from lab analyses of a specific batch. For each Resin, Podophyllum 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.
Resin, Podophyllum may be tested according to a variety of international standards, such as European Pharmacopoeia (Resin, Podophyllum EP), Resin, Podophyllum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Resin, Podophyllum USP).
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