Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONSUS Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
FDF
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for pharmaceutical and biotech industries. LGM also operates as a full-service CDMO, offering formulat...
Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.
About the Company : Nanjing Well Pharmaceutical Group was established in 2000 & is committed to R&D & manufacture of pharmaceutical materials, base oils of advanced synthetic lubricants, etc. The grou...
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...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
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]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - SOLUTION;INTRAVENOUS - 180MG/18ML (1...DOSAGE - SOLUTION;INTRAVENOUS - 180MG/18ML (10MG/ML)
USFDA APPLICATION NUMBER - 205098
DOSAGE - SOLUTION;INTRAVENOUS - 77.5MG/7.75ML...DOSAGE - SOLUTION;INTRAVENOUS - 77.5MG/7.75ML (10MG/ML)
USFDA APPLICATION NUMBER - 205098
DOSAGE - SOLUTION;INTRAVENOUS - 10MG/2ML (5MG...DOSAGE - SOLUTION;INTRAVENOUS - 10MG/2ML (5MG/ML)
USFDA APPLICATION NUMBER - 21201
DOSAGE - SOLUTION;INTRAVENOUS - 20MG/2ML (10M...DOSAGE - SOLUTION;INTRAVENOUS - 20MG/2ML (10MG/ML)
USFDA APPLICATION NUMBER - 21201
Related Excipient Companies
Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Parenteral
Topical
Digital Content
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
Market Place
ABOUT THIS PAGE
52
PharmaCompass offers a list of Polidocanol 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 Polidocanol manufacturer or Polidocanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Polidocanol manufacturer or Polidocanol supplier.
PharmaCompass also assists you with knowing the Polidocanol API Price utilized in the formulation of products. Polidocanol API Price is not always fixed or binding as the Polidocanol Price is obtained through a variety of data sources. The Polidocanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A atossisclerol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of atossisclerol, including repackagers and relabelers. The FDA regulates atossisclerol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. atossisclerol 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 atossisclerol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A atossisclerol supplier is an individual or a company that provides atossisclerol active pharmaceutical ingredient (API) or atossisclerol finished formulations upon request. The atossisclerol suppliers may include atossisclerol API manufacturers, exporters, distributors and traders.
click here to find a list of atossisclerol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A atossisclerol DMF (Drug Master File) is a document detailing the whole manufacturing process of atossisclerol active pharmaceutical ingredient (API) in detail. Different forms of atossisclerol DMFs exist exist since differing nations have different regulations, such as atossisclerol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A atossisclerol DMF submitted to regulatory agencies in the US is known as a USDMF. atossisclerol USDMF includes data on atossisclerol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The atossisclerol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of atossisclerol suppliers with USDMF on PharmaCompass.
atossisclerol 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 atossisclerol 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 atossisclerol GMP manufacturer or atossisclerol GMP API supplier for your needs.
A atossisclerol CoA (Certificate of Analysis) is a formal document that attests to atossisclerol's compliance with atossisclerol specifications and serves as a tool for batch-level quality control.
atossisclerol CoA mostly includes findings from lab analyses of a specific batch. For each atossisclerol 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.
atossisclerol may be tested according to a variety of international standards, such as European Pharmacopoeia (atossisclerol EP), atossisclerol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (atossisclerol USP).
