
USFDA APPLICATION NUMBER - 20865 / DOSAGE - TABLET, ORALLY DISINTEGRATING;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| rizatriptan benzoate(UNII: WR978S7QHH) (rizatriptan - UNII:51086HBW8G) | rizatriptan | 5mg | 10mg | 5mg | 10mg |
Inactive Ingredients
| Ingredient Name | Merck Sharp & Dohme Corp. | Par Pharmaceutical Inc. |
|---|---|---|
| aspartame(Z0H242BBR1) | ||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
| FERRIC OXIDE RED(1K09F3G675) | ||
| gelatin(2G86QN327L) | ||
| gelatin, unspecified(2G86QN327L) | ||
| glycine(TE7660XO1C) | ||
| lactose monohydrate(EWQ57Q8I5X) | ||
| magnesium stearate(70097M6I30) | ||
| mannitol(3OWL53L36A) | ||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
| STARCH, CORN(O8232NY3SJ) |