| NDC Code | 58118-1516-8 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (58118-1516-8) |
|---|
| Product NDC | 58118-1516 |
|---|
| 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 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA019123 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 600 |
|---|
| Strength Unit | mg/1 |
|---|
| 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] |
|---|