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Looking for 1088-11-5 / Nordazepam API manufacturers, exporters & distributors?

Nordazepam manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Nordazepam

Synonyms

Nordiazepam, Desmethyldiazepam, Dealkylprazepam, Norprazepam, N-desmethyldiazepam, 1088-11-5

Cas Number

1088-11-5

Unique Ingredient Identifier (UNII)

67220MCM01

About Nordazepam

An intermediate in the metabolism of DIAZEPAM to OXAZEPAM. It may have actions similar to those of diazepam.

1088-11-5 Manufacturers

A 1088-11-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1088-11-5, including repackagers and relabelers. The FDA regulates 1088-11-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1088-11-5 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 1088-11-5 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

1088-11-5 Suppliers

A 1088-11-5 supplier is an individual or a company that provides 1088-11-5 active pharmaceutical ingredient (API) or 1088-11-5 finished formulations upon request. The 1088-11-5 suppliers may include 1088-11-5 API manufacturers, exporters, distributors and traders.

click here to find a list of 1088-11-5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

1088-11-5 WC

A 1088-11-5 written confirmation (1088-11-5 WC) is an official document issued by a regulatory agency to a 1088-11-5 manufacturer, verifying that the manufacturing facility of a 1088-11-5 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 1088-11-5 APIs or 1088-11-5 finished pharmaceutical products to another nation, regulatory agencies frequently require a 1088-11-5 WC (written confirmation) as part of the regulatory process.

click here to find a list of 1088-11-5 suppliers with Written Confirmation (WC) on PharmaCompass.

1088-11-5 GMP

1088-11-5 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 1088-11-5 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 1088-11-5 GMP manufacturer or 1088-11-5 GMP API supplier for your needs.

1088-11-5 CoA

A 1088-11-5 CoA (Certificate of Analysis) is a formal document that attests to 1088-11-5's compliance with 1088-11-5 specifications and serves as a tool for batch-level quality control.

1088-11-5 CoA mostly includes findings from lab analyses of a specific batch. For each 1088-11-5 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.

1088-11-5 may be tested according to a variety of international standards, such as European Pharmacopoeia (1088-11-5 EP), 1088-11-5 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1088-11-5 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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