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DYMISTA
DYMISTA - 0037-0245-23 - (Azelastine Hydrochloride and Fluticasone Propionate)
Drug Information of DYMISTA
| Product NDC: | 0037-0245 |
| Proprietary Name: | DYMISTA |
| Non Proprietary Name: | Azelastine Hydrochloride and Fluticasone Propionate |
| Active Ingredient(s): | 137; 50 ug/1; ug/1 & nbsp; Azelastine Hydrochloride and Fluticasone Propionate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DYMISTA
| Product NDC: | 0037-0245 |
| Labeler Name: | Meda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202236 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120501 |
Package Information of DYMISTA
| Package NDC: | 0037-0245-23 |
| Package Description: | 1 BOTTLE, SPRAY in 1 BOX (0037-0245-23) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Information of DYMISTA
| NDC Code | 0037-0245-23 |
| Proprietary Name | DYMISTA |
| Package Description | 1 BOTTLE, SPRAY in 1 BOX (0037-0245-23) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY |
| Product NDC | 0037-0245 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Azelastine Hydrochloride and Fluticasone Propionate |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | NDA |
| Labeler Name | Meda Pharmaceuticals Inc. |
| Substance Name | AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE |
| Strength Number | 137; 50 |
| Strength Unit | ug/1; ug/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
