| NDC Code | 65219-144-10 |
|---|
| Package Description | 10 BAG in 1 CASE (65219-144-10) / 1000 mL in 1 BAG (65219-144-04) |
|---|
| Product NDC | 65219-144 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Potassium Chloride In Dextrose And Sodium Chloride |
|---|
| Non-Proprietary Name | Dextrose Monohydrate, Sodium Chloride, And Potassium Chloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20220826 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213523 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| Substance Name | DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
|---|
| Strength | 50; 1.49; 4.5 |
|---|
| Strength Unit | g/1000mL; g/1000mL; g/1000mL |
|---|
| Pharmacy Classes | Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
|---|