USFDA APPLICATION NUMBER - 21610 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
OXYMORPHONE HYDROCHLORIDE(UNII: 5Y2EI94NBC) (OXYMORPHONE - UNII:9VXA968E0C) | OXYMORPHONE HYDROCHLORIDE | 10mg | 20mg |
Inactive Ingredients
Ingredient Name | Bryant Ranch Prepack | St Marys Medical Park Pharmacy | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
---|---|---|---|
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |||
D&C YELLOW NO. 10(35SW5USQ3G) | |||
FD&C BLUE NO. 1(H3R47K3TBD) | |||
FD&C YELLOW NO. 6(H77VEI93A8) | |||
HYPROMELLOSES(3NXW29V3WO) | |||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |||
METHYLPARABEN(A2I8C7HI9T) | |||
POLYETHYLENE GLYCOL(3WJQ0SDW1A) | |||
POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | |||
POLYSORBATE 80(6OZP39ZG8H) | |||
SODIUM STEARYL FUMARATE(7CV7WJK4UI) | |||
TITANIUM DIOXIDE(15FIX9V2JP) | |||
TRIACETIN(XHX3C3X673) |
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