Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 2Ofichem BV
01 1Magnesium Monoethylfumarate
02 1Magnesium Monoethylfumarate Micronized
01 2Netherlands
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-0527
Start Marketing Date : 2018-07-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
NDC Package Code : 62675-1714
Start Marketing Date : 2018-07-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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.
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.
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).
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.
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.
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.
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