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Looking for 58186-27-9 / Idebenone API manufacturers, exporters & distributors?

Idebenone manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Idebenone 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 Idebenone manufacturer or Idebenone supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Idebenone manufacturer or Idebenone supplier.

PharmaCompass also assists you with knowing the Idebenone API Price utilized in the formulation of products. Idebenone API Price is not always fixed or binding as the Idebenone Price is obtained through a variety of data sources. The Idebenone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Idebenone

Synonyms

58186-27-9, 2-(10-hydroxydecyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione, Idebenona, Idebenonum, Sovrima, Hydroxydecyl ubiquinone

Cas Number

58186-27-9

Unique Ingredient Identifier (UNII)

HB6PN45W4J

MolPort-001-758-008 Manufacturers

A MolPort-001-758-008 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-758-008, including repackagers and relabelers. The FDA regulates MolPort-001-758-008 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-758-008 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 MolPort-001-758-008 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-758-008 Suppliers

A MolPort-001-758-008 supplier is an individual or a company that provides MolPort-001-758-008 active pharmaceutical ingredient (API) or MolPort-001-758-008 finished formulations upon request. The MolPort-001-758-008 suppliers may include MolPort-001-758-008 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-758-008 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-758-008 USDMF

A MolPort-001-758-008 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-758-008 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-758-008 DMFs exist exist since differing nations have different regulations, such as MolPort-001-758-008 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-758-008 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-758-008 USDMF includes data on MolPort-001-758-008's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-758-008 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-758-008 suppliers with USDMF on PharmaCompass.

MolPort-001-758-008 NDC

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 MolPort-001-758-008 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-758-008 API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 MolPort-001-758-008 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain MolPort-001-758-008 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-758-008 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MolPort-001-758-008 suppliers with NDC on PharmaCompass.

MolPort-001-758-008 GMP

MolPort-001-758-008 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 MolPort-001-758-008 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 MolPort-001-758-008 GMP manufacturer or MolPort-001-758-008 GMP API supplier for your needs.

MolPort-001-758-008 CoA

A MolPort-001-758-008 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-758-008's compliance with MolPort-001-758-008 specifications and serves as a tool for batch-level quality control.

MolPort-001-758-008 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-758-008 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.

MolPort-001-758-008 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-758-008 EP), MolPort-001-758-008 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-758-008 USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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