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Looking for 147254-64-6 / Ranirestat API manufacturers, exporters & distributors?

Ranirestat manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Ranirestat

Synonyms

147254-64-6, As-3201, Ranirestat [inn], Z26p56gftv, Chembl334830, (3r)-2'-[(4-bromo-2-fluorophenyl)methyl]spiro[pyrrolidine-3,4'-pyrrolo[1,2-a]pyrazine]-1',2,3',5-tetrone

Cas Number

147254-64-6

Unique Ingredient Identifier (UNII)

Z26P56GFTV

About Ranirestat

Ranirestat is a structurally novel and stereospecifically potent aldose reductase (AKR1B; EC 1.1.1.21) inhibitor, which contains a succinimide ring that undergoes ring-opening at physiological pH levels. It has been used in trials studying the treatment of Mild to Moderate Diabetic Sensorimotor Polyneuropathy.

Ranirestat Manufacturers

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

Ranirestat Suppliers

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

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

Ranirestat USDMF

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

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

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

Ranirestat GMP

Ranirestat 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 Ranirestat 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 Ranirestat GMP manufacturer or Ranirestat GMP API supplier for your needs.

Ranirestat CoA

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

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

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