USFDA APPLICATION NUMBER - 20130 / DOSAGE - TABLET;ORAL-21 - 0.02MG,0.03MG,0.035MG;1MG,1MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
Ingredient Name | Allergan, Inc. | Mayne Pharma Inc. |
---|---|---|
CALCIUM STEARATE(776XM7047L) | ||
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
FERROUS FUMARATE(R5L488RY0Q) | ||
LACTOSE(J2B2A4N98G) | ||
LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
MANNITOL(3OWL53L36A) | ||
POVIDONE(FZ989GH94E) | ||
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | ||
SPEARMINT(J7I2T6IV1N) | ||
STARCH, CORN(O8232NY3SJ) | ||
SUCROSE(C151H8M554) |
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