| NDC Code |
0409-7371-03 |
| Proprietary Name |
Ionosol and Dextrose |
| Package Description |
24 POUCH in 1 CASE (0409-7371-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
| Product NDC |
0409-7371 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM LACTATE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, DIBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Dosage Form Name |
INJECTION, SOLUTION |
| Route Name |
INTRAVENOUS |
| Start Marketing Date |
20110325 |
| Marketing Category Name |
NDA |
| Labeler Name |
Hospira, Inc. |
| Substance Name |
DEXTROSE MONOHYDRATE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; SODIUM LACTATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Strength Number |
5; 53; 100; 100; 180; 280; 16 |
| Strength Unit |
g/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
| Pharmaceutical Classes |
Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |