USFDA APPLICATION NUMBER - 21526 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
ranolazine(UNII: A6IEZ5M406) (ranolazine - UNII:A6IEZ5M406) | ranolazine | 500mg |
Inactive Ingredients
Ingredient Name | Cardinal Health |
---|---|
carnauba wax(R12CBM0EIZ) | |
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
ferric oxide red(1K09F3G675) | |
ferric oxide yellow(EX438O2MRT) | |
HYPROMELLOSE 2910 (5 MPA.S)(R75537T0T4) | |
hypromelloses(3NXW29V3WO) | |
magnesium stearate(70097M6I30) | |
methacrylic acid - Ethyl Acrylate Copolymer (1:1) Type A(NX76LV5T8J) | |
polyethylene glycol 3350(G2M7P15E5P) | |
polyethylene glycol 400(B697894SGQ) | |
POLYVINYL ALCOHOL(532B59J990) | |
sodium hydroxide(55X04QC32I) | |
TALC(7SEV7J4R1U) | |
titanium dioxide(15FIX9V2JP) | |
water(059QF0KO0R) |
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