
USFDA APPLICATION NUMBER - 18401 / DOSAGE - INJECTABLE;INJECTION - EQ 0.3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| buprenorphine hydrochloride(UNII: 56W8MW3EN1) (buprenorphine - UNII:40D3SCR4GZ) | buprenorphine | 0.3mg in 1 |
Inactive Ingredients
| Ingredient Name | Indivior Inc. |
|---|---|
| anhydrous dextrose(5SL0G7R0OK) | |
| hydrochloric acid(QTT17582CB) | |
| water(059QF0KO0R) |