USFDA APPLICATION NUMBER - 201739 / DOSAGE - SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.3MG/DELIVERY
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
EPINEPHRINE(UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) | EPINEPHRINE | 0.3mg | .15mg |
Inactive Ingredients
Ingredient Name | kaleo, Inc | sanofi-aventis U.S. LLC |
---|---|---|
HYDROCHLORIC ACID (QTT17582CB) | ||
HYDROCHLORIC ACID(QTT17582CB) | ||
SODIUM BISULFITE(TZX5469Z6I) | ||
SODIUM CHLORIDE (451W47IQ8X) | ||
SODIUM CHLORIDE(451W47IQ8X) | ||
WATER(059QF0KO0R) |
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