Product NDC: | 55154-9613 |
Proprietary Name: | PULMICORT RESPULES |
Non Proprietary Name: | Budesonide |
Active Ingredient(s): | .5 mg/2mL & nbsp; Budesonide |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-9613 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020929 |
Marketing Category: | NDA |
Start Marketing Date: | 20091120 |
Package NDC: | 55154-9613-5 |
Package Description: | 5 AMPULE in 1 BAG (55154-9613-5) > 2 mL in 1 AMPULE |
NDC Code | 55154-9613-5 |
Proprietary Name | PULMICORT RESPULES |
Package Description | 5 AMPULE in 1 BAG (55154-9613-5) > 2 mL in 1 AMPULE |
Product NDC | 55154-9613 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Budesonide |
Dosage Form Name | SUSPENSION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20091120 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | BUDESONIDE |
Strength Number | .5 |
Strength Unit | mg/2mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |