01 1Macco Organiques, S.R.O.
01 1SODIUM GLYCEROPHOSPHATE
01 1Canada
NDC Package Code : 67706-0024
Start Marketing Date : 2023-09-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sodium Glycerophosphate 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 Sodium Glycerophosphate manufacturer or Sodium Glycerophosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Glycerophosphate API Price utilized in the formulation of products. Sodium Glycerophosphate API Price is not always fixed or binding as the Sodium Glycerophosphate Price is obtained through a variety of data sources. The Sodium Glycerophosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PERIKABIVEN IN PLASTIC CONTAINER-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PERIKABIVEN IN PLASTIC CONTAINER-6, including repackagers and relabelers. The FDA regulates PERIKABIVEN IN PLASTIC CONTAINER-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PERIKABIVEN IN PLASTIC CONTAINER-6 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A PERIKABIVEN IN PLASTIC CONTAINER-6 supplier is an individual or a company that provides PERIKABIVEN IN PLASTIC CONTAINER-6 active pharmaceutical ingredient (API) or PERIKABIVEN IN PLASTIC CONTAINER-6 finished formulations upon request. The PERIKABIVEN IN PLASTIC CONTAINER-6 suppliers may include PERIKABIVEN IN PLASTIC CONTAINER-6 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 PERIKABIVEN IN PLASTIC CONTAINER-6 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PERIKABIVEN IN PLASTIC CONTAINER-6 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 PERIKABIVEN IN PLASTIC CONTAINER-6 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 PERIKABIVEN IN PLASTIC CONTAINER-6 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PERIKABIVEN IN PLASTIC CONTAINER-6 NDC to their finished compounded human drug products, they may choose to do so.
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