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USFDA APPLICATION NUMBER - 20092 / DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| DILTIAZEM HYDROCHLORIDE(UNII: OLH94387TE) (DILTIAZEM - UNII:EE92BBP03H) | DILTIAZEM HYDROCHLORIDE | 120mg | 180mg | 240mg |
Inactive Ingredients
| Ingredient Name | Actavis Pharma, Inc. |
|---|---|
| D&C RED NO. 28(767IP0Y5NH) | |
| D&C YELLOW NO. 10(35SW5USQ3G) | |
| ETHYLCELLULOSES(7Z8S9VYZ4B) | |
| FD&C RED NO. 40(WZB9127XOA) | |
| FERRIC OXIDE RED(1K09F3G675) | |
| GELATIN(2G86QN327L) | |
| HYDROGENATED CASTOR OIL(ZF94AP8MEY) | |
| HYPROMELLOSES(3NXW29V3WO) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MANNITOL(3OWL53L36A) | |
| SILICON DIOXIDE(ETJ7Z6XBU4) | |
| STARCH, CORN(O8232NY3SJ) | |
| TITANIUM DIOXIDE(15FIX9V2JP) |
