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Flunisolide
Flunisolide - 60505-0824-0 - (Flunisolide)
Drug Information of Flunisolide
| Product NDC: | 60505-0824 |
| Proprietary Name: | Flunisolide |
| Non Proprietary Name: | Flunisolide |
| Active Ingredient(s): | 29 ug/1 & nbsp; Flunisolide |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flunisolide
| Product NDC: | 60505-0824 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077436 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070810 |
Package Information of Flunisolide
| Package NDC: | 60505-0824-0 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (60505-0824-0) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Information of Flunisolide
| NDC Code | 60505-0824-0 |
| Proprietary Name | Flunisolide |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (60505-0824-0) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY |
| Product NDC | 60505-0824 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flunisolide |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20070810 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | FLUNISOLIDE |
| Strength Number | 29 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
