01 160929
02 1Merck KGaA
03 1Professional Compounding Centers of America
04 1Quality Chemicals S.L.
01 1Sodium Citrate Dihydrate
02 2Sodium citrate
03 1Trisodium Citrate Dihydrate
01 1Spain
02 1U.S.A
03 1United Kingdom
04 1Blank
NDC Package Code : 14639-6666
Start Marketing Date : 2016-03-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5275
Start Marketing Date : 2025-02-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 56141-005
Start Marketing Date : 2021-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60929-832
Start Marketing Date : 2018-07-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
47
PharmaCompass offers a list of Trisodium Citrate Dihydrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Trisodium Citrate Dihydrate manufacturer or Trisodium Citrate Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trisodium Citrate Dihydrate manufacturer or Trisodium Citrate Dihydrate supplier.
A SODIUM CITRATE, DIHYDRATE, U.S.P. manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM CITRATE, DIHYDRATE, U.S.P., including repackagers and relabelers. The FDA regulates SODIUM CITRATE, DIHYDRATE, U.S.P. manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM CITRATE, DIHYDRATE, U.S.P. 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 CITRATE, DIHYDRATE, U.S.P. manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A SODIUM CITRATE, DIHYDRATE, U.S.P. supplier is an individual or a company that provides SODIUM CITRATE, DIHYDRATE, U.S.P. active pharmaceutical ingredient (API) or SODIUM CITRATE, DIHYDRATE, U.S.P. finished formulations upon request. The SODIUM CITRATE, DIHYDRATE, U.S.P. suppliers may include SODIUM CITRATE, DIHYDRATE, U.S.P. API manufacturers, exporters, distributors and traders.
click here to find a list of SODIUM CITRATE, DIHYDRATE, U.S.P. suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 CITRATE, DIHYDRATE, U.S.P. as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for SODIUM CITRATE, DIHYDRATE, U.S.P. 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 CITRATE, DIHYDRATE, U.S.P. 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 CITRATE, DIHYDRATE, U.S.P. and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a SODIUM CITRATE, DIHYDRATE, U.S.P. NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of SODIUM CITRATE, DIHYDRATE, U.S.P. suppliers with NDC on PharmaCompass.
We have 3 companies offering SODIUM CITRATE, DIHYDRATE, U.S.P.
Get in contact with the supplier of your choice:
