USFDA APPLICATION NUMBER - 21860 / DOSAGE - TABLET;ORAL - EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
FLUOXETINE HYDROCHLORIDE(UNII: I9W7N6B1KJ) (FLUOXETINE - UNII:01K63SUP8D) | FLUOXETINE | 20mg | 15mg | 10mg |
Inactive Ingredients
Ingredient Name | Allergan, Inc. |
---|---|
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
CROSCARMELLOSE SODIUM(M28OL1HH48) | |
D&C YELLOW NO. 10(35SW5USQ3G) | |
FD&C YELLOW NO. 6(H77VEI93A8) | |
MAGNESIUM STEARATE(70097M6I30) | |
SILICON DIOXIDE(ETJ7Z6XBU4) |
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