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Looking for 1264-62-6 / Erythromycin Ethyl Succinate API manufacturers, exporters & distributors?

Erythromycin Ethyl Succinate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate manufacturer or Erythromycin Ethyl Succinate supplier for your needs.

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

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

API | Excipient name

Erythromycin Ethyl Succinate

Synonyms

1264-62-6, Erythroped, Pediamycin, Eryped, Wyamycin e, Erythromycin, 2'-(ethyl butanedioate)

Cas Number

1264-62-6

Unique Ingredient Identifier (UNII)

1014KSJ86F

About Erythromycin Ethyl Succinate

A macrolide antibiotic, produced by Streptomyces erythreus. This compound is an ester of erythromycin base and succinic acid. It acts primarily as a bacteriostatic agent. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins.

Erythromycin Ethylsuccinate Manufacturers

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

Erythromycin Ethylsuccinate Suppliers

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

click here to find a list of Erythromycin Ethylsuccinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Erythromycin Ethylsuccinate USDMF

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

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

click here to find a list of Erythromycin Ethylsuccinate suppliers with USDMF on PharmaCompass.

Erythromycin Ethylsuccinate JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Erythromycin Ethylsuccinate Drug Master File in Japan (Erythromycin Ethylsuccinate JDMF) empowers Erythromycin Ethylsuccinate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Erythromycin Ethylsuccinate JDMF during the approval evaluation for pharmaceutical products. At the time of Erythromycin Ethylsuccinate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Erythromycin Ethylsuccinate suppliers with JDMF on PharmaCompass.

Erythromycin Ethylsuccinate CEP

A Erythromycin Ethylsuccinate CEP of the European Pharmacopoeia monograph is often referred to as a Erythromycin Ethylsuccinate Certificate of Suitability (COS). The purpose of a Erythromycin Ethylsuccinate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Erythromycin Ethylsuccinate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Erythromycin Ethylsuccinate to their clients by showing that a Erythromycin Ethylsuccinate CEP has been issued for it. The manufacturer submits a Erythromycin Ethylsuccinate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Erythromycin Ethylsuccinate CEP holder for the record. Additionally, the data presented in the Erythromycin Ethylsuccinate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Erythromycin Ethylsuccinate DMF.

A Erythromycin Ethylsuccinate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Erythromycin Ethylsuccinate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Erythromycin Ethylsuccinate suppliers with CEP (COS) on PharmaCompass.

Erythromycin Ethylsuccinate WC

A Erythromycin Ethylsuccinate written confirmation (Erythromycin Ethylsuccinate WC) is an official document issued by a regulatory agency to a Erythromycin Ethylsuccinate manufacturer, verifying that the manufacturing facility of a Erythromycin Ethylsuccinate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Erythromycin Ethylsuccinate APIs or Erythromycin Ethylsuccinate finished pharmaceutical products to another nation, regulatory agencies frequently require a Erythromycin Ethylsuccinate WC (written confirmation) as part of the regulatory process.

click here to find a list of Erythromycin Ethylsuccinate suppliers with Written Confirmation (WC) on PharmaCompass.

Erythromycin Ethylsuccinate 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 Erythromycin Ethylsuccinate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Erythromycin Ethylsuccinate 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 Erythromycin Ethylsuccinate 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 Erythromycin Ethylsuccinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Erythromycin Ethylsuccinate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Erythromycin Ethylsuccinate suppliers with NDC on PharmaCompass.

Erythromycin Ethylsuccinate GMP

Erythromycin Ethylsuccinate 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 Erythromycin Ethylsuccinate 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 Erythromycin Ethylsuccinate GMP manufacturer or Erythromycin Ethylsuccinate GMP API supplier for your needs.

Erythromycin Ethylsuccinate CoA

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

Erythromycin Ethylsuccinate CoA mostly includes findings from lab analyses of a specific batch. For each Erythromycin Ethylsuccinate 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.

Erythromycin Ethylsuccinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Erythromycin Ethylsuccinate EP), Erythromycin Ethylsuccinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Erythromycin Ethylsuccinate 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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