
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NUMBER - 20142 / DOSAGE - TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |