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USFDA APPLICATION NUMBER - 19697 / DOSAGE - TABLET;ORAL-28 - 0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
| Ingredient Name | Janssen 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) |
