0990-7901Level 3
Potassium Chloride in Dextrose and Sodium Chloride (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE)
**Product type:** Human Prescription Drug
**Active ingredient:** DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
**Strength:** 50; 1.49; 2.25 g/1000mL; g/1000mL; g/1000mL
**Dosage form:** Injection, Solution
**Route:** Intravenous
**Labeler:** ICU Medical Inc.
**Marketing category:** NDA (NDA018365)
**Pharmacologic class:** Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
GET
/api/v1/systems/ndc_fda/nodes/0990-7901Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.