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Looking for 5700-49-2 / Ethylene Diamine Dihydro Iodide API manufacturers, exporters & distributors?

Ethylene Diamine Dihydro Iodide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ethylene Diamine Dihydro Iodide 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 Ethylene Diamine Dihydro Iodide manufacturer or Ethylene Diamine Dihydro Iodide supplier for your needs.

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

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

API | Excipient name

Ethylene Diamine Dihydro Iodide

Synonyms

5700-49-2, Jodethamine, Ethane-1,2-diamine dihydroiodide, Ethanediamine dihydroiodide, Hydrodine, Eddi

Cas Number

5700-49-2

Unique Ingredient Identifier (UNII)

721M52NQ5L

Ethylene Diamine Dihydro Iodide Manufacturers

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

Ethylene Diamine Dihydro Iodide Suppliers

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

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

Ethylene Diamine Dihydro Iodide GMP

Ethylene Diamine Dihydro Iodide 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 Ethylene Diamine Dihydro Iodide 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 Ethylene Diamine Dihydro Iodide GMP manufacturer or Ethylene Diamine Dihydro Iodide GMP API supplier for your needs.

Ethylene Diamine Dihydro Iodide CoA

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

Ethylene Diamine Dihydro Iodide CoA mostly includes findings from lab analyses of a specific batch. For each Ethylene Diamine Dihydro Iodide 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.

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