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Looking for 77191-36-7 / Nefiracetam API manufacturers, exporters & distributors?

Nefiracetam manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Nefiracetam

Synonyms

77191-36-7, N-(2,6-dimethylphenyl)-2-(2-oxopyrrolidin-1-yl)acetamide, Translon, Dm 9384, Nefiracetam [inn], Motiva

Cas Number

77191-36-7

Unique Ingredient Identifier (UNII)

1JK12GX30N

About Nefiracetam

Nefiracetam has been used in trials studying the treatment of Alzheimer's Disease.

Nefiracetam Manufacturers

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

Nefiracetam Suppliers

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

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

Nefiracetam USDMF

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

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

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

Nefiracetam GMP

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

Nefiracetam CoA

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

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

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