0264-7636Level 3
Potassium Chloride in Dextrose and Sodium Chloride (DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE)
**Product type:** Human Prescription Drug
**Active ingredient:** DEXTROSE, UNSPECIFIED FORM; POTASSIUM CHLORIDE; SODIUM CHLORIDE
**Strength:** 5; .22; .45 g/100mL; g/100mL; g/100mL
**Dosage form:** Injection
**Route:** Intravenous
**Labeler:** B. Braun Medical Inc.
**Marketing category:** NDA (NDA019630)
**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/0264-7636Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.