46163-300Level 3
Sodium Chloride (Sodium Chloride)
**Product type:** Human Prescription Drug
**Active ingredient:** SODIUM CHLORIDE
**Strength:** 900 mg/100mL
**Dosage form:** Injection
**Route:** Intravenous
**Labeler:** Fresenius Medical Care de Mexico, S.A. de C.V.
**Marketing category:** ANDA (ANDA078177)
**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/46163-300Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.