
USFDA APPLICATION NUMBER - 21235 / DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 90mg | 
Inactive Ingredients
| Ingredient Name | Eli Lilly and Company  | 
					
|---|---|
| D&C Yellow No. 10(35SW5USQ3G) | |
| FD&C Blue No. 2(L06K8R7DQK) | |
| FERROSOFERRIC OXIDE(XM0M87F357) | |
| Gelatin(2G86QN327L) | |
| HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)(24P2YXD2PW) | |
| Hypromelloses(3NXW29V3WO) | |
| Sodium lauryl sulfate(368GB5141J) | |
| Sucrose(C151H8M554) | |
| Talc(7SEV7J4R1U) | |
| Titanium dioxide(15FIX9V2JP) | |
| Triethyl citrate(8Z96QXD6UM) |