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Laboratorium Ofichem BV

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Laboratorium Ofichem BV

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MAGNESIUM MONOETHYLFUMARATE

NDC Package Code : 62675-0527

Start Marketing Date : 2018-07-02

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Laboratorium Ofichem BV

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Laboratorium Ofichem BV

Country
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MAGNESIUM MONOETHYLFUMARATE

NDC Package Code : 62675-1714

Start Marketing Date : 2018-07-02

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Looking for 83918-60-9 / Magnesium Monoethylfumarate API manufacturers, exporters & distributors?

Magnesium Monoethylfumarate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Magnesium Monoethylfumarate

Synonyms

83918-60-9, Magnesium;(e)-4-ethoxy-4-oxobut-2-enoate, D5767608s8, Monoethyl fumarate magnesium, Fumaric acid monoethyl ester magnesium salt (2:1), Fumaric acid monoethyl ester magnesium salt

Cas Number

83918-60-9

Unique Ingredient Identifier (UNII)

D5767608S8

Magnesium Monoethylfumarate Manufacturers

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

Magnesium Monoethylfumarate Suppliers

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

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

Magnesium Monoethylfumarate 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 Magnesium Monoethylfumarate as an active pharmaceutical ingredient (API).

Finished drug products

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

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

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.