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Looking for 71771-90-9 / Denopamine API manufacturers, exporters & distributors?

Denopamine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Denopamine

Synonyms

71771-90-9, R(-)-denopamine, Kalgut, Ta 064, Ta-064, 4-[(1r)-2-[2-(3,4-dimethoxyphenyl)ethylamino]-1-hydroxyethyl]phenol

Cas Number

71771-90-9

Unique Ingredient Identifier (UNII)

V5F60UPD8P

Denopamine Manufacturers

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

Denopamine Suppliers

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

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

Denopamine JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Denopamine Drug Master File in Japan (Denopamine JDMF) empowers Denopamine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Denopamine JDMF during the approval evaluation for pharmaceutical products. At the time of Denopamine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Denopamine suppliers with JDMF on PharmaCompass.

Denopamine GMP

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

Denopamine CoA

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

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

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