
USFDA APPLICATION NUMBER - 21947 / DOSAGE - TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 
|---|---|---|
| FENTANYL CITRATE(UNII: MUN5LYG46H) (FENTANYL - UNII:UF599785JZ)  | FENTANYL | 100ug | 200ug | 400ug | 600ug | 800ug | 
Inactive Ingredients
| Ingredient Name | Teva Pharmaceuticals USA, Inc.  | 
					
|---|---|
| ANHYDROUS CITRIC ACID(XF417D3PSL) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MANNITOL(3OWL53L36A) | |
| SODIUM BICARBONATE(8MDF5V39QO) | |
| SODIUM CARBONATE(45P3261C7T) | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) |