| NDC Code | 52584-965-02 |
|---|
| Package Description | 1 VIAL in 1 BAG (52584-965-02) > 20 mL in 1 VIAL |
|---|
| Product NDC | 52584-965 |
|---|
| 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 | 20191213 |
|---|
| End Marketing Date | 20231130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA088901 |
|---|
| Manufacturer | General Injectables & Vaccines, Inc. |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | meq/mL |
|---|
| 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] |
|---|