USFDA APPLICATION NUMBER - 18703 / DOSAGE - TABLET;ORAL - EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
RANITIDINE HYDROCHLORIDE(UNII: BK76465IHM) (RANITIDINE - UNII:884KT10YB7) | RANITIDINE | 300mg | 150mg |
Inactive Ingredients
Ingredient Name | GlaxoSmithKline LLC |
---|---|
CROSCARMELLOSE SODIUM(M28OL1HH48) | |
D&C YELLOW NO. 10(35SW5USQ3G) | |
FD&C YELLOW NO. 6(H77VEI93A8) | |
FERRIC OXIDE YELLOW(EX438O2MRT) | |
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
MAGNESIUM STEARATE(70097M6I30) | |
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
TITANIUM DIOXIDE(15FIX9V2JP) | |
TRIACETIN(XHX3C3X673) |
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