USFDA APPLICATION NUMBER - 21001 / DOSAGE - TABLET;ORAL - EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
almotriptan malate(UNII: PJP312605E) (almotriptan - UNII:1O4XL5SN61) | almotriptan | 12.5mg | 6.25mg |
Inactive Ingredients
Ingredient Name | Janssen Pharmaceuticals, Inc. | Patriot Pharmaceuticals, LLC |
---|---|---|
carnauba wax(R12CBM0EIZ) | ||
FD&C Blue No. 2(L06K8R7DQK) | ||
ferric oxide red(1K09F3G675) | ||
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | ||
mannitol(3OWL53L36A) | ||
POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | ||
POVIDONE, UNSPECIFIED(FZ989GH94E) | ||
powdered cellulose(SMD1X3XO9M) | ||
propylene glycol(6DC9Q167V3) | ||
sodium starch glycolate type A potato(5856J3G2A2) | ||
sodium stearyl fumarate(7CV7WJK4UI) | ||
titanium dioxide(15FIX9V2JP) |
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