NDC 24208-344
Flunisolide
Flunisolide
Flunisolide is a Nasal Solution in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Flunisolide.
| Product ID | 24208-344_cd97aa97-0d80-4f70-8c74-461caa23e12b |
| NDC | 24208-344 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Flunisolide |
| Generic Name | Flunisolide |
| Dosage Form | Solution |
| Route of Administration | NASAL |
| Marketing Start Date | 2002-02-20 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074805 |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | FLUNISOLIDE |
| Active Ingredient Strength | 0 mg/mL |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |