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Looking for 59-47-2 / Mephenesin API manufacturers, exporters & distributors?

Mephenesin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Mephenesin

Synonyms

59-47-2, Cresoxydiol, Decontractyl, Memphenesin, Mephenesine, Mephedan

Cas Number

59-47-2

Unique Ingredient Identifier (UNII)

7B8PIR2954

About Mephenesin

A centrally acting muscle relaxant with a short duration of action.

Prestwick3_000178 Manufacturers

A Prestwick3_000178 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000178, including repackagers and relabelers. The FDA regulates Prestwick3_000178 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000178 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 Prestwick3_000178 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Prestwick3_000178 Suppliers

A Prestwick3_000178 supplier is an individual or a company that provides Prestwick3_000178 active pharmaceutical ingredient (API) or Prestwick3_000178 finished formulations upon request. The Prestwick3_000178 suppliers may include Prestwick3_000178 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_000178 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_000178 WC

A Prestwick3_000178 written confirmation (Prestwick3_000178 WC) is an official document issued by a regulatory agency to a Prestwick3_000178 manufacturer, verifying that the manufacturing facility of a Prestwick3_000178 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prestwick3_000178 APIs or Prestwick3_000178 finished pharmaceutical products to another nation, regulatory agencies frequently require a Prestwick3_000178 WC (written confirmation) as part of the regulatory process.

click here to find a list of Prestwick3_000178 suppliers with Written Confirmation (WC) on PharmaCompass.

Prestwick3_000178 GMP

Prestwick3_000178 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 Prestwick3_000178 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 Prestwick3_000178 GMP manufacturer or Prestwick3_000178 GMP API supplier for your needs.

Prestwick3_000178 CoA

A Prestwick3_000178 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_000178's compliance with Prestwick3_000178 specifications and serves as a tool for batch-level quality control.

Prestwick3_000178 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_000178 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.

Prestwick3_000178 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_000178 EP), Prestwick3_000178 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_000178 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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