01 1Chongqing Biocare Pharmaceutical Ltd.
02 1JQC (Huayin) Pharmaceutical Co., Ltd.
03 1JQC(Huayin) Pharmaceutical Co.,Ltd
04 1Professional Compounding Centers of America dba PCCA
05 1SALICYLATES & CHEMICALS PRIVATE LIMITED
06 1Spectrum Laboratory Products, Inc.
01 3SODIUM SALICYLATE
02 3Sodium Salicylate
01 2China
02 1India
03 1U.S.A
04 1United Kingdom
05 1Blank
NDC Package Code : 14534-222
Start Marketing Date : 2019-10-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14534-222
Start Marketing Date : 2002-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1679
Start Marketing Date : 2024-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 76107-225
Start Marketing Date : 2018-09-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6990
Start Marketing Date : 1989-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 33656-0008
Start Marketing Date : 2017-07-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Sodium Salicylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Salicylate, including repackagers and relabelers. The FDA regulates Sodium Salicylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Salicylate 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 Salicylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Salicylate supplier is an individual or a company that provides Sodium Salicylate active pharmaceutical ingredient (API) or Sodium Salicylate finished formulations upon request. The Sodium Salicylate suppliers may include Sodium Salicylate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Salicylate 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 Salicylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Salicylate 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 Salicylate 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 Salicylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Salicylate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Salicylate suppliers with NDC on PharmaCompass.
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