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PULMICORT RESPULES
PULMICORT RESPULES - 0186-1988-04 - (Budesonide)
Drug Information of PULMICORT RESPULES
| Product NDC: | 0186-1988 |
| Proprietary Name: | PULMICORT RESPULES |
| Non Proprietary Name: | Budesonide |
| Active Ingredient(s): | .25 mg/2mL & nbsp; Budesonide |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PULMICORT RESPULES
| Product NDC: | 0186-1988 |
| Labeler Name: | AstraZeneca LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020929 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000908 |
Package Information of PULMICORT RESPULES
| Package NDC: | 0186-1988-04 |
| Package Description: | 6 POUCH in 1 CARTON (0186-1988-04) > 5 AMPULE in 1 POUCH > 2 mL in 1 AMPULE |
NDC Information of PULMICORT RESPULES
| NDC Code | 0186-1988-04 |
| Proprietary Name | PULMICORT RESPULES |
| Package Description | 6 POUCH in 1 CARTON (0186-1988-04) > 5 AMPULE in 1 POUCH > 2 mL in 1 AMPULE |
| Product NDC | 0186-1988 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Budesonide |
| Dosage Form Name | SUSPENSION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20000908 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca LP |
| Substance Name | BUDESONIDE |
| Strength Number | .25 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
