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RHINOCORT AQUA
RHINOCORT AQUA - 0186-1070-08 - (Budesonide)
Drug Information of RHINOCORT AQUA
| Product NDC: | 0186-1070 |
| Proprietary Name: | RHINOCORT AQUA |
| Non Proprietary Name: | Budesonide |
| Active Ingredient(s): | 32 ug/1 & nbsp; Budesonide |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RHINOCORT AQUA
| Product NDC: | 0186-1070 |
| Labeler Name: | AstraZeneca LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020746 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010402 |
Package Information of RHINOCORT AQUA
| Package NDC: | 0186-1070-08 |
| Package Description: | 120 SPRAY, METERED in 1 BOTTLE, SPRAY (0186-1070-08) |
NDC Information of RHINOCORT AQUA
| NDC Code | 0186-1070-08 |
| Proprietary Name | RHINOCORT AQUA |
| Package Description | 120 SPRAY, METERED in 1 BOTTLE, SPRAY (0186-1070-08) |
| Product NDC | 0186-1070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Budesonide |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20010402 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca LP |
| Substance Name | BUDESONIDE |
| Strength Number | 32 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
