| NDC Code | 68382-853-77 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68382-853-77) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68382-853-30) |
|---|
| Product NDC | 68382-853 |
|---|
| 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 | 20190630 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208445 |
|---|
| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
|---|
| 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] |
|---|