65219-230Level 3
Sodium chloride (SODIUM CHLORIDE)
**Product type:** Human Prescription Drug
**Active ingredient:** SODIUM CHLORIDE
**Strength:** 1125 mg/250mL
**Dosage form:** Injection, Solution
**Route:** Intravenous
**Labeler:** Fresenius Kabi USA, LLC
**Marketing category:** ANDA (ANDA208122)
**Pharmacologic class:** Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
GET
/api/v1/systems/ndc_fda/nodes/65219-230Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.