NORMOSOL-M AND DEXTROSE (dextrose monohydrate, sodium chloride, potassium acetate, and magnesium acetate)
**Product type:** Human Prescription Drug
**Active ingredient:** DEXTROSE MONOHYDRATE; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE
**Strength:** 5; 21; 128; 234 g/100mL; mg/100mL; mg/100mL; mg/100mL
**Dosage form:** Injection, Solution
**Route:** Intravenous
**Labeler:** ICU Medical Inc.
**Marketing category:** NDA (NDA017610)
**Pharmacologic class:** Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
/api/v1/systems/ndc_fda/nodes/0990-7965Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.