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Looking for 69542-93-4 / Pivagabine API manufacturers, exporters & distributors?

Pivagabine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Pivagabine

Synonyms

69542-93-4, 4-pivalamidobutanoic acid, 4-[(2,2-dimethylpropanoyl)amino]butanoic acid, Cxb-722, Pivagabine [inn], 4-(2,2-dimethylpropanoylamino)butanoic acid

Cas Number

69542-93-4

Unique Ingredient Identifier (UNII)

C53SV0WO4V

About Pivagabine

Pivagabine has been used in trials studying the treatment of Stress and Anxiety.

Pivagabine Manufacturers

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

Pivagabine Suppliers

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

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

Pivagabine USDMF

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

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

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

Pivagabine GMP

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

Pivagabine CoA

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

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

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