USFDA APPLICATION NUMBER - 20142 / DOSAGE - TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
DICLOFENAC POTASSIUM(UNII: L4D5UA6CB4) (DICLOFENAC - UNII:144O8QL0L1) | DICLOFENAC POTASSIUM | 50mg |
Inactive Ingredients
Ingredient Name | Novartis Pharmaceuticals Corporation |
---|---|
CALCIUM PHOSPHATE(97Z1WI3NDX) | |
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
FERRIC OXIDE RED(1K09F3G675) | |
MAGNESIUM STEARATE(70097M6I30) | |
POLYETHYLENE GLYCOL(3WJQ0SDW1A) | |
POVIDONE(FZ989GH94E) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | |
STARCH, CORN(O8232NY3SJ) | |
SUCROSE(C151H8M554) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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