USFDA APPLICATION NUMBER - 21277 / DOSAGE - SOLUTION;INTRAVENOUS - 400MG/250ML (1.6MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
MOXIFLOXACIN HYDROCHLORIDE(UNII: C53598599T) (MOXIFLOXACIN - UNII:U188XYD42P) | MOXIFLOXACIN | 400mg | 400mg in 250 |
Inactive Ingredients
Ingredient Name | Schering Plough Corporation | Bayer HealthCare Pharmaceuticals Inc. |
---|---|---|
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
CROSCARMELLOSE SODIUM(M28OL1HH48) | ||
FERRIC OXIDE RED(1K09F3G675) | ||
HYDROCHLORIC ACID(QTT17582CB) | ||
HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | ||
HYPROMELLOSES(3NXW29V3WO) | ||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | ||
POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | ||
SODIUM CHLORIDE(451W47IQ8X) | ||
SODIUM HYDROXIDE(55X04QC32I) | ||
TITANIUM DIOXIDE(15FIX9V2JP) | ||
WATER(059QF0KO0R) |
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