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USFDA APPLICATION NUMBER - 21695 / DOSAGE - CAPSULE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| FENOFIBRATE(UNII: U202363UOS) (FENOFIBRIC ACID - UNII:BGF9MN2HU1) | FENOFIBRATE | 30mg | 90mg |
Inactive Ingredients
| Ingredient Name | Lupin Pharmaceuticals, Inc. |
|---|---|
| D&C YELLOW NO. 10(35SW5USQ3G) | |
| DIMETHICONE(92RU3N3Y1O) | |
| FD&C BLUE NO. 1(H3R47K3TBD) | |
| FD&C BLUE NO. 2(L06K8R7DQK) | |
| FD&C YELLOW NO. 6(H77VEI93A8) | |
| FERRIC OXIDE YELLOW(EX438O2MRT) | |
| FERROSOFERRIC OXIDE(XM0M87F357) | |
| GELATIN(2G86QN327L) | |
| HYPROMELLOSES(3NXW29V3WO) | |
| LECITHIN, SOYBEAN(1DI56QDM62) | |
| POTASSIUM HYDROXIDE(WZH3C48M4T) | |
| PROPYLENE GLYCOL(6DC9Q167V3) | |
| SHELLAC(46N107B71O) | |
| SODIUM LAURYL SULFATE(368GB5141J) | |
| SUCROSE(C151H8M554) | |
| SULFUR DIOXIDE(0UZA3422Q4) | |
| TALC(7SEV7J4R1U) | |
| TITANIUM DIOXIDE(15FIX9V2JP) |
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