| NDC Code | 70436-001-02 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-001-02) |
|---|
| Product NDC | 70436-001 |
|---|
| 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 | 20181115 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209314 |
|---|
| Manufacturer | Slate Run Pharmaceuticals, LLC |
|---|
| Substance Name | POTASSIUM CHLORIDE |
|---|
| Strength | 600 |
|---|
| 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] |
|---|