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Looking for 77-21-4 / Glutethimide API manufacturers, exporters & distributors?

Glutethimide manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Glutethimide

Synonyms

Doriden, Elrodorm, Noxyron, Sarodormin, Glutethimid, Glutetimid

Cas Number

77-21-4

Unique Ingredient Identifier (UNII)

C8I4BVN78E

About Glutethimide

A hypnotic and sedative. Its use has been largely superseded by other drugs.

Glutethimide Manufacturers

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

Glutethimide Suppliers

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

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

Glutethimide USDMF

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

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

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

Glutethimide GMP

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

Glutethimide CoA

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

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

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