"0409-7965-09" National Drug Code (NDC)

NDC Code	0409-7965-09
Package Description	12 POUCH in 1 CASE (0409-7965-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG
Product NDC	0409-7965
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Normosol-m And Dextrose
Non-Proprietary Name	Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, And Magnesium Acetate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	19750813
End Marketing Date	20210501
Marketing Category Name	NDA
Application Number	NDA017610
Manufacturer	Hospira, Inc.
Substance Name	DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM ACETATE; MAGNESIUM ACETATE
Strength	5; 234; 128; 21
Strength Unit	g/100mL; mg/100mL; mg/100mL; mg/100mL
Pharmacy Classes	Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]