
USFDA APPLICATION NUMBER - 19152 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| VERAPAMIL HYDROCHLORIDE(UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) | VERAPAMIL HYDROCHLORIDE | 240mg | 180mg | 120mg |
Inactive Ingredients
| Ingredient Name | Pfizer Laboratories Div Pfizer Inc |
|---|---|
| CARNAUBA WAX(R12CBM0EIZ) | |
| D&C YELLOW NO. 10(35SW5USQ3G) | |
| FD&C BLUE NO. 2(L06K8R7DQK) | |
| FERRIC OXIDE RED(1K09F3G675) | |
| HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |
| SODIUM ALGINATE(C269C4G2ZQ) | |
| TALC(7SEV7J4R1U) | |
| TITANIUM DIOXIDE(15FIX9V2JP) |