USFDA APPLICATION NUMBER - 213224 / DOSAGE - SOLUTION;SUBCUTANEOUS - 7MG/2.8ML (2.5MG/ML)
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
OCTREOTIDE ACETATE(UNII: 75R0U2568I) (OCTREOTIDE - UNII:RWM8CCW8GP) | OCTREOTIDE | 2.5mg in 1 |
Inactive Ingredients
Ingredient Name | Sun Pharmaceutical Industries, Inc. |
---|---|
LACTIC ACID(33X04XA5AT) | |
MANNITOL(3OWL53L36A) | |
PHENOL(339NCG44TV) | |
SODIUM BICARBONATE(8MDF5V39QO) | |
WATER(059QF0KO0R) |
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