USFDA APPLICATION NUMBER - 18817 / DOSAGE - TABLET;ORAL - 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 120mg | 80mg |
Inactive Ingredients
Ingredient Name | G.D. Searle LLC Division of Pfizer Inc |
---|---|
GELATIN, UNSPECIFIED(2G86QN327L) | |
HYDROXYPROPYL CELLULOSE (1600000 WAMW)(RFW2ET671P) | |
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
MAGNESIUM STEARATE(70097M6I30) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |
STARCH, CORN(O8232NY3SJ) | |
TALC(7SEV7J4R1U) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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