
USFDA APPLICATION NUMBER - 20746 / DOSAGE - SPRAY, METERED;NASAL - 0.032MG/SPRAY
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| BUDESONIDE(UNII: Q3OKS62Q6X) (BUDESONIDE - UNII:Q3OKS62Q6X)  | BUDESONIDE | 32ug | 
Inactive Ingredients
| Ingredient Name | Apotex Corp.  | AstraZeneca Pharmaceuticals LP  | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division  | Par Pharmaceutical Inc.  | Rite Aid  | Topco Associates LLC  | Amerisource Bergen  | CVS Pharmacy  | Rugby Laboratories  | Safeway  | 
					
|---|---|---|---|---|---|---|---|---|---|---|
| anhydrous dextrose(5SL0G7R0OK) | ||||||||||
| CARBOXYMETHYLCELLULOSE SODIUM(K679OBS311) | ||||||||||
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (K679OBS311) | ||||||||||
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | ||||||||||
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED(K679OBS311) | ||||||||||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||||||||||
| DEXTROSE(IY9XDZ35W2) | ||||||||||
| DEXTROSE, UNSPECIFIED FORM (IY9XDZ35W2) | ||||||||||
| DEXTROSE, UNSPECIFIED FORM(IY9XDZ35W2) | ||||||||||
| EDETATE DISODIUM(7FLD91C86K) | ||||||||||
| HYDROCHLORIC ACID(QTT17582CB) | ||||||||||
| MICROCRYSTALLINE CELLULOSE (OP1R32D61U) | ||||||||||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||||||||||
| POLYSORBATE 80(6OZP39ZG8H) | ||||||||||
| POTASSIUM SORBATE(1VPU26JZZ4) | ||||||||||
| WATER(059QF0KO0R) |