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