SPI Pharma has been solving formulation challenges using superior functional materials.
01 2SPI Pharma
02 1Elementis Pharma Gmbh
01 3Magaldrate
01 1Germany
02 2U.S.A
SPI Pharma has been solving formulation challenges using superior functional materials.
NDC Package Code : 12784-204
Start Marketing Date : 2014-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (98kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
SPI Pharma has been solving formulation challenges using superior functional materials.
NDC Package Code : 12784-205
Start Marketing Date : 2020-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (98kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 55603-170
Start Marketing Date : 2013-11-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Magaldrate 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 Magaldrate manufacturer or Magaldrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magaldrate manufacturer or Magaldrate supplier.
PharmaCompass also assists you with knowing the Magaldrate API Price utilized in the formulation of products. Magaldrate API Price is not always fixed or binding as the Magaldrate Price is obtained through a variety of data sources. The Magaldrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glysan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glysan, including repackagers and relabelers. The FDA regulates Glysan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glysan 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 Glysan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glysan supplier is an individual or a company that provides Glysan active pharmaceutical ingredient (API) or Glysan finished formulations upon request. The Glysan suppliers may include Glysan API manufacturers, exporters, distributors and traders.
click here to find a list of Glysan 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 Glysan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glysan 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 Glysan 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 Glysan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glysan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glysan suppliers with NDC on PharmaCompass.
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