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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) |
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