01 1Jost Chemical Co.
01 1Calcium Phosphate Dibasic Anhydrous
01 1U.S.A
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
NDC Package Code : 55570-180
Start Marketing Date : 2008-02-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Calcium Acid Phosphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Calcium Acid Phosphate manufacturer or Calcium Acid Phosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Calcium Acid Phosphate API Price utilized in the formulation of products. Calcium Acid Phosphate API Price is not always fixed or binding as the Calcium Acid Phosphate Price is obtained through a variety of data sources. The Calcium Acid Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biofos manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biofos, including repackagers and relabelers. The FDA regulates Biofos manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biofos 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 Biofos manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biofos supplier is an individual or a company that provides Biofos active pharmaceutical ingredient (API) or Biofos finished formulations upon request. The Biofos suppliers may include Biofos API manufacturers, exporters, distributors and traders.
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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 Biofos as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Biofos 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 Biofos 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 Biofos and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Biofos NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Biofos suppliers with NDC on PharmaCompass.
