
USFDA APPLICATION NUMBER - 201739 / DOSAGE - SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS - EQ 0.1MG/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) |