| NDC Code | 54868-0767-1 |
|---|
| Package Description | 16 CONTAINER in 1 CASE (54868-0767-1) > 25 VIAL in 1 CONTAINER > 10 mL in 1 VIAL |
|---|
| Product NDC | 54868-0767 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Potassium Chloride |
|---|
| Non-Proprietary Name | Potassium Chloride |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20070316 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA080205 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 149 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
|---|