| NDC Code | 0781-1526-01 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-1526-01) |
|---|
| Product NDC | 0781-1526 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Potassium Chloride |
|---|
| Non-Proprietary Name | Potassium Chloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19860417 |
|---|
| End Marketing Date | 20220228 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA019123 |
|---|
| Manufacturer | Sandoz Inc. |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 750 |
|---|
| Strength Unit | mg/1 |
|---|
| 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] |
|---|