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Looking for 82964-04-3 / Tolrestat API manufacturers, exporters & distributors?

Tolrestat manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Tolrestat

Synonyms

82964-04-3, Alredase, Lorestat, Tolrestatin, Ay-27773, Tolrestatum

Cas Number

82964-04-3

Unique Ingredient Identifier (UNII)

0T93LG5NMK

About Tolrestat

Tolrestat (INN) (AY-27773) is an aldose reductase inhibitor which was approved for the control of certain diabetic complications. While it was approved for marketed in several countries, it failed a Phase III trial in the U.S. due to toxicity and never received FDA approval. It was sold under the tradename Alredase but was discontinued by Wyeth in 1997 because of the risk of severe liver toxicity and death.

Alredasereg Manufacturers

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

Alredasereg Suppliers

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

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

Alredasereg USDMF

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

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

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

Alredasereg GMP

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

Alredasereg CoA

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

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

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