01 1Fagron Inc
01 1Dextrose Anhydrous
01 1Netherlands
NDC Package Code : 51552-0458
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-07-06
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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A TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1, including repackagers and relabelers. The FDA regulates TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 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 TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 supplier is an individual or a company that provides TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 active pharmaceutical ingredient (API) or TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 finished formulations upon request. The TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 suppliers may include TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 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 TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 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 TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 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 TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER-1 NDC to their finished compounded human drug products, they may choose to do so.
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