| NDC Code | 53808-1125-1 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-1125-1) |
|---|
| Product NDC | 53808-1125 |
|---|
| 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 | 20180524 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204662 |
|---|
| Manufacturer | DOH CENTRAL PHARMACY |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | meq/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] |
|---|