| NDC Code |
0338-0143-03 |
| Proprietary Name |
Dextrose and Electrolyte No. 48 |
| Package Description |
500 mL in 1 BAG (0338-0143-03) |
| Product NDC |
0338-0143 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phosphate, Sodium Chloride and Dextrose monohydrate |
| Dosage Form Name |
INJECTION, SOLUTION |
| Route Name |
INTRAVENOUS |
| Start Marketing Date |
19790202 |
| Marketing Category Name |
NDA |
| Labeler Name |
Baxter Healthcare Company |
| Substance Name |
DEXTROSE MONOHYDRATE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE |
| Strength Number |
5; 31; 141; 20; 12; 260 |
| Strength Unit |
g/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] |