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USFDA APPLICATION NUMBER - 213224 / DOSAGE - SOLUTION;SUBCUTANEOUS - EQ 7MG BASE/2.8ML (EQ 2.5MG BASE/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) |
