| NDC Code | 53808-0277-1 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0277-1) |
|---|
| Product NDC | 53808-0277 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | K-tab |
|---|
| Non-Proprietary Name | Potassium Chloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090701 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA018279 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 750 |
|---|
| 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] |
|---|