
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- 21860 / DOSAGE - TABLET;ORAL - EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |