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Looking for 60-40-2 / Mecamylamine API manufacturers, exporters & distributors?

Mecamylamine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Mecamylamine

Synonyms

Versamine, Mecamine, Revertina, Mecamilamina, Mekamine, 60-40-2

Cas Number

60-40-2

About Mecamylamine

A nicotinic antagonist that is well absorbed from the gastrointestinal tract and crosses the blood-brain barrier. Mecamylamine has been used as a ganglionic blocker in treating hypertension, but, like most ganglionic blockers, is more often used now as a research tool.

Prestwick2_001111 Manufacturers

A Prestwick2_001111 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick2_001111, including repackagers and relabelers. The FDA regulates Prestwick2_001111 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick2_001111 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Prestwick2_001111 Suppliers

A Prestwick2_001111 supplier is an individual or a company that provides Prestwick2_001111 active pharmaceutical ingredient (API) or Prestwick2_001111 finished formulations upon request. The Prestwick2_001111 suppliers may include Prestwick2_001111 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick2_001111 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick2_001111 USDMF

A Prestwick2_001111 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick2_001111 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick2_001111 DMFs exist exist since differing nations have different regulations, such as Prestwick2_001111 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick2_001111 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick2_001111 USDMF includes data on Prestwick2_001111's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick2_001111 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick2_001111 suppliers with USDMF on PharmaCompass.

Prestwick2_001111 GMP

Prestwick2_001111 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 Prestwick2_001111 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 Prestwick2_001111 GMP manufacturer or Prestwick2_001111 GMP API supplier for your needs.

Prestwick2_001111 CoA

A Prestwick2_001111 CoA (Certificate of Analysis) is a formal document that attests to Prestwick2_001111's compliance with Prestwick2_001111 specifications and serves as a tool for batch-level quality control.

Prestwick2_001111 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick2_001111 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.

Prestwick2_001111 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick2_001111 EP), Prestwick2_001111 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick2_001111 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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