USFDA APPLICATION NUMBER - 203667 / DOSAGE - TABLET;ORAL - 0.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
Ingredient Name | Actavis Pharma, Inc. |
---|---|
ACACIA(5C5403N26O) | |
FERROUS FUMARATE(R5L488RY0Q) | |
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |
MAGNESIUM STEARATE(70097M6I30) | |
MANNITOL(3OWL53L36A) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
POVIDONE, UNSPECIFIED(FZ989GH94E) | |
SODIUM STARCH GLYCOLATE TYPE A CORN(AG9B65PV6B) | |
STARCH, CORN(O8232NY3SJ) | |
SUCRALOSE(96K6UQ3ZD4) | |
SUCROSE(C151H8M554) | |
TALC(7SEV7J4R1U) |
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