63323-867Level 3
Dextrose and Sodium Chloride (DEXTROSE MONOHYDRATE and SODIUM CHLORIDE)
**Product type:** Human Prescription Drug
**Active ingredient:** DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
**Strength:** 5; .3 g/100mL; g/100mL
**Dosage form:** Injection, Solution
**Route:** Intravenous
**Labeler:** Fresenius Kabi USA, LLC
**Marketing category:** ANDA (ANDA211194)
**Pharmacologic class:** Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
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