| NDC Code | 68382-320-01 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-320-01) |
|---|
| Product NDC | 68382-320 |
|---|
| 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 | 20170601 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA018279 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA 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] |
|---|