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USFDA APPLICATION NUMBER - 18238 / DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| POTASSIUM CHLORIDE(UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM CHLORIDE | 750mg |
Inactive Ingredients
| Ingredient Name | American Health Packaging | McKesson Contract Packaging | NCS HealthCare of KY, Inc dba Vangard Labs | REMEDYREPACK INC. | Zydus Pharmaceuticals (USA) Inc. | REMEDYREPACK INC. |
|---|---|---|---|---|---|---|
| ALUMINUM OXIDE(LMI26O6933) | ||||||
| ETHYLCELLULOSES(7Z8S9VYZ4B) | ||||||
| FD&C BLUE NO. 2(L06K8R7DQK) | ||||||
| FD&C RED NO. 40(WZB9127XOA) | ||||||
| FD&C YELLOW NO. 6(H77VEI93A8) | ||||||
| GELATIN(2G86QN327L) | ||||||
| MAGNESIUM STEARATE(70097M6I30) | ||||||
| SODIUM LAURYL SULFATE(368GB5141J) | ||||||
| TITANIUM DIOXIDE(15FIX9V2JP) |
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