USFDA APPLICATION NUMBER - 216142 / DOSAGE - SOLUTION;INTRAVENOUS - EQ 100MG BASE/100ML (EQ 1MG BASE/ML)
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
MICAFUNGIN SODIUM(UNII: IS1UP79R56) (MICAFUNGIN - UNII:R10H71BSWG) | MICAFUNGIN SODIUM | 150mg in 150 | 100mg in 100 | 50mg in 50 |
Inactive Ingredients
Ingredient Name | Baxter Healthcare Corporation |
---|---|
ANHYDROUS CITRIC ACID(XF417D3PSL) | |
SODIUM CHLORIDE(451W47IQ8X) | |
TRISODIUM CITRATE DIHYDRATE(B22547B95K) | |
WATER(059QF0KO0R) |
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