01 1Macco Organiques, S.R.O.
02 1Macco Organiques, S.r.o.
01 2SODIUM SULFATE ANHYDROUS
01 2Canada
NDC Package Code : 67706-0022
Start Marketing Date : 2021-10-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67706-0004
Start Marketing Date : 2014-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Sodium Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Sulfate, including repackagers and relabelers. The FDA regulates Sodium Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Sulfate 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 Sodium Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Sulfate supplier is an individual or a company that provides Sodium Sulfate active pharmaceutical ingredient (API) or Sodium Sulfate finished formulations upon request. The Sodium Sulfate suppliers may include Sodium Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Sulfate 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 Sodium Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Sulfate 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 Sodium Sulfate 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 Sodium Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Sulfate suppliers with NDC on PharmaCompass.
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