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PharmaCompass offers a list of Carbopol 940 API 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 Carbopol 940 API manufacturer or Carbopol 940 API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbopol 940 API manufacturer or Carbopol 940 API supplier.
PharmaCompass also assists you with knowing the Carbopol 940 API API Price utilized in the formulation of products. Carbopol 940 API API Price is not always fixed or binding as the Carbopol 940 API Price is obtained through a variety of data sources. The Carbopol 940 API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Carbopol 940 API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbopol 940 API, including repackagers and relabelers. The FDA regulates Carbopol 940 API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbopol 940 API 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 Carbopol 940 API supplier is an individual or a company that provides Carbopol 940 API active pharmaceutical ingredient (API) or Carbopol 940 API finished formulations upon request. The Carbopol 940 API suppliers may include Carbopol 940 API API manufacturers, exporters, distributors and traders.
click here to find a list of Carbopol 940 API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carbopol 940 API DMF (Drug Master File) is a document detailing the whole manufacturing process of Carbopol 940 API active pharmaceutical ingredient (API) in detail. Different forms of Carbopol 940 API DMFs exist exist since differing nations have different regulations, such as Carbopol 940 API USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carbopol 940 API DMF submitted to regulatory agencies in the US is known as a USDMF. Carbopol 940 API USDMF includes data on Carbopol 940 API's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carbopol 940 API USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carbopol 940 API suppliers with USDMF 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 Carbopol 940 API as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Carbopol 940 API 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 Carbopol 940 API 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 Carbopol 940 API and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Carbopol 940 API NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Carbopol 940 API suppliers with NDC on PharmaCompass.
Carbopol 940 API 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 Carbopol 940 API 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 Carbopol 940 API GMP manufacturer or Carbopol 940 API GMP API supplier for your needs.
A Carbopol 940 API CoA (Certificate of Analysis) is a formal document that attests to Carbopol 940 API's compliance with Carbopol 940 API specifications and serves as a tool for batch-level quality control.
Carbopol 940 API CoA mostly includes findings from lab analyses of a specific batch. For each Carbopol 940 API 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.
Carbopol 940 API may be tested according to a variety of international standards, such as European Pharmacopoeia (Carbopol 940 API EP), Carbopol 940 API JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Carbopol 940 API USP).
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