USFDA APPLICATION NUMBER - 18985 / DOSAGE - TABLET;ORAL-28 - 0.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
Ingredient Name | Actavis Pharma, Inc. | Janssen Pharmaceuticals, Inc. |
---|---|---|
ALUMINUM OXIDE(LMI26O6933) | ||
D&C YELLOW No. 10(35SW5USQ3G) | ||
FD&C BLUE No. 2(L06K8R7DQK) | ||
FD&C YELLOW No. 6(H77VEI93A8) | ||
LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
STARCH, CORN(O8232NY3SJ) |
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