USFDA APPLICATION NUMBER - 22008 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
ROPINIROLE HYDROCHLORIDE(UNII: D7ZD41RZI9) (ROPINIROLE - UNII:030PYR8953) | ROPINIROLE | 12mg | 8mg | 6mg | 4mg | 2mg |
Inactive Ingredients
Ingredient Name | Glaxo Wellcome SA | GlaxoSmithKline LLC |
---|---|---|
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | ||
FD&C BLUE NO. 2(L06K8R7DQK) | ||
FD&C YELLOW NO. 6(H77VEI93A8) | ||
FERRIC OXIDE RED(1K09F3G675) | ||
FERRIC OXIDE YELLOW(EX438O2MRT) | ||
GLYCERYL DIBEHENATE(R8WTH25YS2) | ||
HYDROGENATED CASTOR OIL(ZF94AP8MEY) | ||
HYPROMELLOSE 2910 (6 MPA.S)(0WZ8WG20P6) | ||
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | ||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
MALTODEXTRIN(7CVR7L4A2D) | ||
MANNITOL(3OWL53L36A) | ||
POLYETHYLENE GLYCOL 400(B697894SGQ) | ||
POVIDONE, UNSPECIFIED(FZ989GH94E) | ||
SILICON DIOXIDE(ETJ7Z6XBU4) | ||
TITANIUM DIOXIDE(15FIX9V2JP) |
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