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USFDA APPLICATION NUMBER - 19667 / DOSAGE - INJECTABLE;INJECTION - EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| OCTREOTIDE ACETATE(UNII: 75R0U2568I) (OCTREOTIDE - UNII:RWM8CCW8GP) | OCTREOTIDE | 1000ug in 1 | 200ug in 1 |
Inactive Ingredients
| Ingredient Name | Sandoz Inc |
|---|---|
| LACTIC ACID(33X04XA5AT) | |
| MANNITOL(3OWL53L36A) | |
| PHENOL(339NCG44TV) | |
| SODIUM BICARBONATE(8MDF5V39QO) | |
| WATER(059QF0KO0R) |
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