01 1Spectrum Laboratory Products, Inc.
01 1D-Panthenol
01 1U.S.A
NDC Package Code : 49452-2464
Start Marketing Date : 2024-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1.2kg/L)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of D-Panthenol 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 D-Panthenol manufacturer or D-Panthenol supplier for your needs.
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PharmaCompass also assists you with knowing the D-Panthenol API Price utilized in the formulation of products. D-Panthenol API Price is not always fixed or binding as the D-Panthenol Price is obtained through a variety of data sources. The D-Panthenol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4, including repackagers and relabelers. The FDA regulates INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 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 INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 supplier is an individual or a company that provides INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 active pharmaceutical ingredient (API) or INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 finished formulations upon request. The INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 suppliers may include INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 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 INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 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 INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 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 INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a INFUVITE PEDIATRIC (PHARMACY BULK PACKAGE)-4 NDC to their finished compounded human drug products, they may choose to do so.
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