01 1Jost Chemical Co.
01 1Calcium Hydroxide
01 1U.S.A
NDC Package Code : 55570-160
Start Marketing Date : 2008-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Calcium Hydroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Hydroxide, including repackagers and relabelers. The FDA regulates Calcium Hydroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Hydroxide 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 Hydroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Hydroxide supplier is an individual or a company that provides Calcium Hydroxide active pharmaceutical ingredient (API) or Calcium Hydroxide finished formulations upon request. The Calcium Hydroxide suppliers may include Calcium Hydroxide API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Hydroxide 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 Hydroxide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Calcium Hydroxide 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 Hydroxide 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 Hydroxide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Calcium Hydroxide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Calcium Hydroxide suppliers with NDC on PharmaCompass.
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