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Looking for 51-60-5 / Neostigmine Methyl Sulfate API manufacturers, exporters & distributors?

Neostigmine Methyl Sulfate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate manufacturer or Neostigmine Methyl Sulfate supplier for your needs.

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

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

API | Excipient name

Neostigmine Methyl Sulfate

Synonyms

51-60-5, Syntostigmin, Normastigmin, Hodostin, Neostigmine methylsulphate, Neostigmine metilsulfate

Cas Number

51-60-5

Unique Ingredient Identifier (UNII)

98IMH7M386

About Neostigmine Methyl Sulfate

A cholinesterase inhibitor used in the treatment of myasthenia gravis and to reverse the effects of muscle relaxants such as gallamine and tubocurarine. Neostigmine, unlike PHYSOSTIGMINE, does not cross the blood-brain barrier.

Neostigmine Methyl Sulfate Manufacturers

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

Neostigmine Methyl Sulfate Suppliers

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

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

Neostigmine Methyl Sulfate USDMF

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

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

click here to find a list of Neostigmine Methyl Sulfate suppliers with USDMF on PharmaCompass.

Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate Drug Master File in Japan (Neostigmine Methyl Sulfate JDMF) empowers Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate suppliers with JDMF on PharmaCompass.

Neostigmine Methyl Sulfate CEP

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

A Neostigmine Methyl Sulfate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate suppliers with CEP (COS) on PharmaCompass.

Neostigmine Methyl Sulfate WC

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

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

Neostigmine Methyl Sulfate NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Neostigmine Methyl Sulfate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Neostigmine Methyl Sulfate API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Neostigmine Methyl Sulfate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Neostigmine Methyl Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Neostigmine Methyl Sulfate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Neostigmine Methyl Sulfate suppliers with NDC on PharmaCompass.

Neostigmine Methyl Sulfate GMP

Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate GMP manufacturer or Neostigmine Methyl Sulfate GMP API supplier for your needs.

Neostigmine Methyl Sulfate CoA

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

Neostigmine Methyl Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Neostigmine Methyl Sulfate 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.

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