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Looking for 13755-41-4 / UNII-I670EI8M2N API manufacturers, exporters & distributors?

UNII-I670EI8M2N manufacturers, exporters & distributors 1

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PharmaCompass offers a list of UNII-I670EI8M2N 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 UNII-I670EI8M2N manufacturer or UNII-I670EI8M2N supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred UNII-I670EI8M2N manufacturer or UNII-I670EI8M2N supplier.

PharmaCompass also assists you with knowing the UNII-I670EI8M2N API Price utilized in the formulation of products. UNII-I670EI8M2N API Price is not always fixed or binding as the UNII-I670EI8M2N Price is obtained through a variety of data sources. The UNII-I670EI8M2N Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

UNII-I670EI8M2N

Synonyms

Tasto, 13755-41-4, I670ei8m2n, Tris(hydroxymethyl)aminomethanegluconate dihydroxyaluminate, Aluminum;2-amino-2-(hydroxymethyl)propane-1,3-diol;(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoate;dihydroxide, Aloglutamol [who-dd]

Cas Number

13755-41-4

Unique Ingredient Identifier (UNII)

I670EI8M2N

UNII-I670EI8M2N Manufacturers

A UNII-I670EI8M2N manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-I670EI8M2N, including repackagers and relabelers. The FDA regulates UNII-I670EI8M2N manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-I670EI8M2N API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

UNII-I670EI8M2N Suppliers

A UNII-I670EI8M2N supplier is an individual or a company that provides UNII-I670EI8M2N active pharmaceutical ingredient (API) or UNII-I670EI8M2N finished formulations upon request. The UNII-I670EI8M2N suppliers may include UNII-I670EI8M2N API manufacturers, exporters, distributors and traders.

click here to find a list of UNII-I670EI8M2N suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

UNII-I670EI8M2N USDMF

A UNII-I670EI8M2N DMF (Drug Master File) is a document detailing the whole manufacturing process of UNII-I670EI8M2N active pharmaceutical ingredient (API) in detail. Different forms of UNII-I670EI8M2N DMFs exist exist since differing nations have different regulations, such as UNII-I670EI8M2N USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A UNII-I670EI8M2N DMF submitted to regulatory agencies in the US is known as a USDMF. UNII-I670EI8M2N USDMF includes data on UNII-I670EI8M2N's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The UNII-I670EI8M2N USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of UNII-I670EI8M2N suppliers with USDMF on PharmaCompass.

UNII-I670EI8M2N GMP

UNII-I670EI8M2N 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 UNII-I670EI8M2N 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 UNII-I670EI8M2N GMP manufacturer or UNII-I670EI8M2N GMP API supplier for your needs.

UNII-I670EI8M2N CoA

A UNII-I670EI8M2N CoA (Certificate of Analysis) is a formal document that attests to UNII-I670EI8M2N's compliance with UNII-I670EI8M2N specifications and serves as a tool for batch-level quality control.

UNII-I670EI8M2N CoA mostly includes findings from lab analyses of a specific batch. For each UNII-I670EI8M2N 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.

UNII-I670EI8M2N may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-I670EI8M2N EP), UNII-I670EI8M2N JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-I670EI8M2N 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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