01 2B.V. KATWIJK CHEMIE
02 1Fagron Inc
03 1Fagron Services B.V.
04 1Jiangsu Tianhe Pharmaceutical Co., Ltd.
05 1KATWIJK CHEMIE BV
06 1MEDISCA Inc
07 1Professional Compounding Centers of America dba PCCA
08 1Spectrum Laboratory Products, Inc.
09 1Xenex Laboratories Inc
01 4SULFACETAMIDE SODIUM
02 1SULFACETAMIDE SODIUM MONOHYDRATE
03 3Sulfacetamide Sodium
04 1Sulfacetamide Sodium Crystals
05 1Sulfacetamide sodium
01 1Canada
02 1China
03 5Netherlands
04 2U.S.A
05 1United Kingdom
NDC Package Code : 76003-1054
Start Marketing Date : 2020-07-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51552-0244
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-10-13
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17349-0010
Start Marketing Date : 1984-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17349-0022
Start Marketing Date : 1984-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17349-0001
Start Marketing Date : 1984-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0049
Start Marketing Date : 2015-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1053
Start Marketing Date : 2013-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-7450
Start Marketing Date : 1990-02-01
End Marketing Date : 2026-05-06
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69169-118
Start Marketing Date : 2021-03-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68981-042
Start Marketing Date : 2021-04-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Sulfacetamide Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfacetamide Sodium, including repackagers and relabelers. The FDA regulates Sulfacetamide Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfacetamide Sodium 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 Sulfacetamide Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulfacetamide Sodium supplier is an individual or a company that provides Sulfacetamide Sodium active pharmaceutical ingredient (API) or Sulfacetamide Sodium finished formulations upon request. The Sulfacetamide Sodium suppliers may include Sulfacetamide Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfacetamide Sodium 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 Sulfacetamide Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulfacetamide Sodium 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 Sulfacetamide Sodium 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 Sulfacetamide Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulfacetamide Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulfacetamide Sodium suppliers with NDC on PharmaCompass.
We have 7 companies offering Sulfacetamide Sodium
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
