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PULMICORT
PULMICORT - 0186-0916-12 - (Budesonide)
Drug Information of PULMICORT
| Product NDC: | 0186-0916 |
| Proprietary Name: | PULMICORT |
| Non Proprietary Name: | Budesonide |
| Active Ingredient(s): | 180 ug/1 & nbsp; Budesonide |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | AEROSOL, POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PULMICORT
| Product NDC: | 0186-0916 |
| Labeler Name: | AstraZeneca LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021949 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070319 |
Package Information of PULMICORT
| Package NDC: | 0186-0916-12 |
| Package Description: | 1 INHALER in 1 CARTON (0186-0916-12) > 120 AEROSOL, POWDER in 1 INHALER |
NDC Information of PULMICORT
| NDC Code | 0186-0916-12 |
| Proprietary Name | PULMICORT |
| Package Description | 1 INHALER in 1 CARTON (0186-0916-12) > 120 AEROSOL, POWDER in 1 INHALER |
| Product NDC | 0186-0916 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Budesonide |
| Dosage Form Name | AEROSOL, POWDER |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20070319 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca LP |
| Substance Name | BUDESONIDE |
| Strength Number | 180 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
