01 2Jost Chemical Co.
01 1Ferrous Sulfate Heptahydrate
02 1Ferrous Sulfate, Dried
01 2U.S.A
NDC Package Code : 55570-245
Start Marketing Date : 2018-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55570-246
Start Marketing Date : 2018-05-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sorbifer durules manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sorbifer durules, including repackagers and relabelers. The FDA regulates Sorbifer durules manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sorbifer durules 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 Sorbifer durules manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sorbifer durules supplier is an individual or a company that provides Sorbifer durules active pharmaceutical ingredient (API) or Sorbifer durules finished formulations upon request. The Sorbifer durules suppliers may include Sorbifer durules API manufacturers, exporters, distributors and traders.
click here to find a list of Sorbifer durules 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 Sorbifer durules as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sorbifer durules 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 Sorbifer durules 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 Sorbifer durules and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sorbifer durules NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sorbifer durules suppliers with NDC on PharmaCompass.
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