01 1Spectrum Laboratory Products, Inc.
01 1Sodium DL-Lactate Solution
01 1U.S.A
NDC Package Code : 49452-6830
Start Marketing Date : 1986-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.6kg/L)
Marketing Category : DRUG FOR FURTHER PROCESSING
100
PharmaCompass offers a list of Sodium Lactate 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 Lactate manufacturer or Sodium Lactate supplier for your needs.
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A DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4, including repackagers and relabelers. The FDA regulates DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 supplier is an individual or a company that provides DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 active pharmaceutical ingredient (API) or DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 finished formulations upon request. The DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 suppliers may include DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 NDC to their finished compounded human drug products, they may choose to do so.
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