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Looking for 31377-23-8 / Amantadine Sulphate API manufacturers, exporters & distributors?

Amantadine Sulphate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Amantadine Sulphate

Synonyms

31377-23-8, Amantadine (sulfate), 31377-23-8 (sulfate), Tricyclo[3.3.1.13,7]decan-1-amine, sulfate (2:1), Tricyclo(3.3.1.1(3,7))decan-1-amine, sulfate (2:1), 9921t5p019

Cas Number

31377-23-8

Unique Ingredient Identifier (UNII)

9921T5P019

About Amantadine Sulphate

An antiviral that is used in the prophylactic or symptomatic treatment of influenza A. It is also used as an antiparkinsonian agent, to treat extrapyramidal reactions, and for postherpetic neuralgia. The mechanisms of its effects in movement disorders are not well understood but probably reflect an increase in synthesis and release of dopamine, with perhaps some inhibition of dopamine uptake.

Amantadine Sulphate Manufacturers

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

Amantadine Sulphate Suppliers

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

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

Amantadine Sulphate 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 Amantadine Sulphate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Amantadine Sulphate 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 Amantadine Sulphate 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 Amantadine Sulphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amantadine Sulphate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Amantadine Sulphate suppliers with NDC on PharmaCompass.

Amantadine Sulphate GMP

Amantadine Sulphate 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 Amantadine Sulphate 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 Amantadine Sulphate GMP manufacturer or Amantadine Sulphate GMP API supplier for your needs.

Amantadine Sulphate CoA

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

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

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