Budesonide
- Product NDC
- 50090-1467
- 11-digit product format
- 500901467
- Labeler code
- 50090
- Product ID
- 50090-1467_ab2faae8-3e28-451b-b901-a9b24fe0e104
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- SUSPENSION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- ANDA077519
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- Substance
- BUDESONIDE
- Active strength
- .25 mg/2mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Q3OKS62Q6X | BUDESONIDE | 51333-22-3 | BUDESONIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-1467-0 | 50090146700 | 30 VIAL in 1 CARTON (50090-1467-0) / 2 mL in 1 VIAL | 30 vial | 2014-11-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Budesonide | A-S Medication Solutions | 2023-11-29 | HUMAN PRESCRIPTION DRUG LABEL | 2 |