
USFDA APPLICATION NUMBER - 200677 / DOSAGE - SOLUTION;SUBCUTANEOUS - EQ 0.6MG BASE/ML (EQ 0.6MG BASE/ML)
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| PASIREOTIDE(UNII: 98H1T17066) (PASIREOTIDE - UNII:98H1T17066) | PASIREOTIDE | 0.9mg in 1 | 0.6mg in 1 | 0.3mg in 1 |
Inactive Ingredients
| Ingredient Name | Novartis Pharmaceuticals Corporation |
|---|---|
| MANNITOL(3OWL53L36A) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| TARTARIC ACID(W4888I119H) | |
| WATER(059QF0KO0R) |