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USFDA APPLICATION NUMBER - 19462 / DOSAGE - TABLET;ORAL - 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| FAMOTIDINE(UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) | FAMOTIDINE | 20mg |
Inactive Ingredients
| Ingredient Name | PD-Rx Pharmaceuticals, Inc. |
|---|---|
| CARNAUBA WAX(R12CBM0EIZ) | |
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
| FERRIC OXIDE RED(1K09F3G675) | |
| FERRIC OXIDE YELLOW(EX438O2MRT) | |
| HYDROXYPROPYL CELLULOSE(RFW2ET671P) | |
| HYPROMELLOSES(3NXW29V3WO) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| STARCH, CORN(O8232NY3SJ) | |
| TALC(7SEV7J4R1U) | |
| TITANIUM DIOXIDE(15FIX9V2JP) |
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