USFDA APPLICATION NUMBER - 200677 / DOSAGE - SOLUTION;SUBCUTANEOUS - EQ 0.9MG BASE/ML (EQ 0.9MG 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) |
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