| NDC Code | 0409-7924-03 | 
|---|
			| Package Description | 24 POUCH in 1 CASE (0409-7924-03)  > 1 BAG in 1 POUCH > 500 mL in 1 BAG | 
|---|
			| Product NDC | 0409-7924 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Dextrose And Sodium Chloride | 
|---|
			
			| Non-Proprietary Name | Dextrose Monohydrate And Sodium Chloride | 
|---|
			| Dosage Form | INJECTION, SOLUTION | 
|---|
			| Usage | INTRAVENOUS | 
|---|
			| Start Marketing Date | 20050606 | 
|---|
			| End Marketing Date | 20220708 | 
|---|
			| Marketing Category Name | NDA | 
|---|
			| Application Number | NDA017606 | 
|---|
			| Manufacturer | Hospira, Inc. | 
|---|
			| Substance Name | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE | 
|---|
			| Strength | 5; .225 | 
|---|
			| Strength Unit | g/100mL; g/100mL | 
|---|
			| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] | 
|---|