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Looking for 504-24-5 / Dalfampridine API manufacturers, exporters & distributors?

Dalfampridine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dalfampridine

Synonyms

504-24-5, Pyridin-4-amine, Fampridine, 4-pyridinamine, 4-pyridylamine, P-aminopyridine

Cas Number

504-24-5

Unique Ingredient Identifier (UNII)

BH3B64OKL9

About Dalfampridine

One of the POTASSIUM CHANNEL BLOCKERS with secondary effect on calcium currents which is used mainly as a research tool and to characterize channel subtypes.

AM20061261 Manufacturers

A AM20061261 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20061261, including repackagers and relabelers. The FDA regulates AM20061261 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20061261 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 AM20061261 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

AM20061261 Suppliers

A AM20061261 supplier is an individual or a company that provides AM20061261 active pharmaceutical ingredient (API) or AM20061261 finished formulations upon request. The AM20061261 suppliers may include AM20061261 API manufacturers, exporters, distributors and traders.

click here to find a list of AM20061261 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

AM20061261 USDMF

A AM20061261 DMF (Drug Master File) is a document detailing the whole manufacturing process of AM20061261 active pharmaceutical ingredient (API) in detail. Different forms of AM20061261 DMFs exist exist since differing nations have different regulations, such as AM20061261 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A AM20061261 DMF submitted to regulatory agencies in the US is known as a USDMF. AM20061261 USDMF includes data on AM20061261's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AM20061261 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of AM20061261 suppliers with USDMF on PharmaCompass.

AM20061261 WC

A AM20061261 written confirmation (AM20061261 WC) is an official document issued by a regulatory agency to a AM20061261 manufacturer, verifying that the manufacturing facility of a AM20061261 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AM20061261 APIs or AM20061261 finished pharmaceutical products to another nation, regulatory agencies frequently require a AM20061261 WC (written confirmation) as part of the regulatory process.

click here to find a list of AM20061261 suppliers with Written Confirmation (WC) on PharmaCompass.

AM20061261 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 AM20061261 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for AM20061261 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 AM20061261 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 AM20061261 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AM20061261 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of AM20061261 suppliers with NDC on PharmaCompass.

AM20061261 GMP

AM20061261 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 AM20061261 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 AM20061261 GMP manufacturer or AM20061261 GMP API supplier for your needs.

AM20061261 CoA

A AM20061261 CoA (Certificate of Analysis) is a formal document that attests to AM20061261's compliance with AM20061261 specifications and serves as a tool for batch-level quality control.

AM20061261 CoA mostly includes findings from lab analyses of a specific batch. For each AM20061261 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.

AM20061261 may be tested according to a variety of international standards, such as European Pharmacopoeia (AM20061261 EP), AM20061261 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AM20061261 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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