USFDA APPLICATION NUMBER - 20864 / DOSAGE - TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 10mg |
Inactive Ingredients
Ingredient Name | Merck Sharp & Dohme Corp. | Par Pharmaceutical Inc. | Lake Erie Medical DBA Quality Care Products LLC |
---|---|---|---|
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) |
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