Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
01 1Pfanstiehl, Inc.
02 1Roquette Freres SA
03 1SMS Pharmaceuticals Limited
01 2SODIUM GLUCONATE
02 1Sodium Gluconate
01 1France
02 1India
03 1U.S.A
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
NDC Package Code : 67430-150
Start Marketing Date : 2017-01-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50516-004
Start Marketing Date : 2020-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0035
Start Marketing Date : 2024-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sodium Gluconate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Gluconate, including repackagers and relabelers. The FDA regulates Sodium Gluconate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Gluconate 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 Gluconate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Gluconate supplier is an individual or a company that provides Sodium Gluconate active pharmaceutical ingredient (API) or Sodium Gluconate finished formulations upon request. The Sodium Gluconate suppliers may include Sodium Gluconate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Gluconate 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 Gluconate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Gluconate 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 Gluconate 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 Gluconate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Gluconate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Gluconate suppliers with NDC on PharmaCompass.
We have 3 companies offering Sodium Gluconate
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