| NDC Code | 51477-002-04 |
|---|
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51477-002-04) |
|---|
| Product NDC | 51477-002 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Potassium Chloride |
|---|
| Non-Proprietary Name | Potassium Chloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101025 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA018238 |
|---|
| Manufacturer | Nesher Pharmaceuticals (USA) LLC |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 600 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
|---|