| NDC Code | 0409-8183-01 |
|---|
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-01) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-11) |
|---|
| Product NDC | 0409-8183 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Potassium Acetate |
|---|
| Non-Proprietary Name | Potassium Acetate |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20050707 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA018896 |
|---|
| Manufacturer | Hospira, Inc. |
|---|
| Substance Name | POTASSIUM ACETATE |
|---|
| Strength | 3.93 |
|---|
| Strength Unit | g/20mL |
|---|
| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
|---|