01 1Macco Organiques, S.R.O.
02 1Professional Compounding Centers of America
01 2CALCIUM CHLORIDE
01 1Canada
02 1United Kingdom
NDC Package Code : 67706-0001
Start Marketing Date : 2014-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0328
Start Marketing Date : 2024-01-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Calcium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Chloride, including repackagers and relabelers. The FDA regulates Calcium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Chloride 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 Calcium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Chloride supplier is an individual or a company that provides Calcium Chloride active pharmaceutical ingredient (API) or Calcium Chloride finished formulations upon request. The Calcium Chloride suppliers may include Calcium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Chloride 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 Calcium Chloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Calcium Chloride 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 Calcium Chloride 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 Calcium Chloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Calcium Chloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Calcium Chloride suppliers with NDC on PharmaCompass.
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