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USFDA APPLICATION NUMBER - 19653 / DOSAGE - TABLET;ORAL-28 - 0.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
| Ingredient Name | Janssen Pharmaceuticals, Inc. | Proficient Rx LP | RPK Pharmaceuticals, Inc. |
|---|---|---|---|
| ALUMINUM OXIDE(LMI26O6933) | |||
| CARNAUBA WAX(R12CBM0EIZ) | |||
| Croscarmellose Sodium(M28OL1HH48) | |||
| FD&C BLUE No. 2(L06K8R7DQK) | |||
| Ferric Oxide Red(1K09F3G675) | |||
| HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |||
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |||
| MAGNESIUM STEARATE(70097M6I30) | |||
| Microcrystalline Cellulose(OP1R32D61U) | |||
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |||
| Polysorbate 80(6OZP39ZG8H) | |||
| POLYVINYL ALCOHOL, UNSPECIFIED(532B59J990) | |||
| STARCH, CORN(O8232NY3SJ) | |||
| TALC(7SEV7J4R1U) | |||
| Titanium Dioxide(15FIX9V2JP) | |||
| Water(059QF0KO0R) |
