All FDA drug approvals

FDA approval · Drugs@FDA

DELFLEX W/ DEXTROSE 2.5% LOW MAGNESIUM IN PLASTIC CONTAINERcalcium chloride, dextrose, magnesium chloride, sodium chloride, sodium lactate

NDA018883 ·

FDA approved the original new drug application for DELFLEX W/ DEXTROSE 2.5% LOW MAGNESIUM IN PLASTIC CONTAINER on November 30, 1984, sponsored by FRESENIUS MEDCL. FDA’s record shows no approved efficacy supplement on the application since.

Application
NDA018883
Sponsor
FRESENIUS MEDCL
Original approval
Review
standard review
Submission class
Type 5 - New Formulation or New Manufacturer
Active ingredient
calcium chloride, dextrose, magnesium chloride, sodium chloride, sodium lactate

Products under this application

Ingredient and strengthFormRouteMarketing status
calcium chloride 25.7MG/100ML; dextrose 2.5GM/100ML; magnesium chloride 5.08MG/100ML; sodium chloride 538MG/100ML; sodium lactate 448MG/100MLSOLUTIONINTRAPERITONEALPrescription
calcium chloride 25.7MG/100ML; dextrose 4.25GM/100ML; magnesium chloride 15.2MG/100ML; sodium chloride 567MG/100ML; sodium lactate 392MG/100MLSOLUTIONINTRAPERITONEALPrescription
calcium chloride 25.7MG/100ML; dextrose 1.5GM/100ML; magnesium chloride 15.2MG/100ML; sodium chloride 567MG/100ML; sodium lactate 392MG/100MLSOLUTIONINTRAPERITONEALPrescription
calcium chloride 25.7MG/100ML; dextrose 4.25GM/100ML; magnesium chloride 5.08MG/100ML; sodium chloride 538MG/100ML; sodium lactate 448MG/100MLSOLUTIONINTRAPERITONEALPrescription
calcium chloride 25.7MG/100ML; dextrose 1.5GM/100ML; magnesium chloride 5.08MG/100ML; sodium chloride 538MG/100ML; sodium lactate 448MG/100MLSOLUTIONINTRAPERITONEALPrescription
calcium chloride 25.7MG/100ML; dextrose 2.5GM/100ML; magnesium chloride 15.2MG/100ML; sodium chloride 567MG/100ML; sodium lactate 392MG/100MLSOLUTIONINTRAPERITONEALPrescription

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

FDA’s record shows no approved efficacy supplement on this application.

FDA records other approved supplements on this application, by the class code it assigns them: Manufacturing (CMC) 32 · Labeling 10. Those are changes to the label or to how the drug is made rather than new clinical evidence, so they are counted here and not listed.

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

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