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Looking for 36105-20-1 / Flurazepam Monohydrochloride API manufacturers, exporters & distributors?

Flurazepam Monohydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Flurazepam Monohydrochloride

Synonyms

36105-20-1, Dalmate, 7c4jh842ij, Dalmadorm, Dalmane, Felison

Cas Number

36105-20-1

Unique Ingredient Identifier (UNII)

7C4JH842IJ

About Flurazepam Monohydrochloride

A benzodiazepine derivative used mainly as a hypnotic.

Flurazepam Monohydrochloride Manufacturers

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

click here to find a list of Flurazepam Monohydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Flurazepam Monohydrochloride Suppliers

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

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

Flurazepam Monohydrochloride CEP

A Flurazepam Monohydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Flurazepam Monohydrochloride Certificate of Suitability (COS). The purpose of a Flurazepam Monohydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flurazepam Monohydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flurazepam Monohydrochloride to their clients by showing that a Flurazepam Monohydrochloride CEP has been issued for it. The manufacturer submits a Flurazepam Monohydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flurazepam Monohydrochloride CEP holder for the record. Additionally, the data presented in the Flurazepam Monohydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flurazepam Monohydrochloride DMF.

A Flurazepam Monohydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flurazepam Monohydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Flurazepam Monohydrochloride suppliers with CEP (COS) on PharmaCompass.

Flurazepam Monohydrochloride WC

A Flurazepam Monohydrochloride written confirmation (Flurazepam Monohydrochloride WC) is an official document issued by a regulatory agency to a Flurazepam Monohydrochloride manufacturer, verifying that the manufacturing facility of a Flurazepam Monohydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Flurazepam Monohydrochloride APIs or Flurazepam Monohydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Flurazepam Monohydrochloride WC (written confirmation) as part of the regulatory process.

click here to find a list of Flurazepam Monohydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.

Flurazepam Monohydrochloride GMP

Flurazepam Monohydrochloride 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 Flurazepam Monohydrochloride 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 Flurazepam Monohydrochloride GMP manufacturer or Flurazepam Monohydrochloride GMP API supplier for your needs.

Flurazepam Monohydrochloride CoA

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

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

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