Budesonide
- Product NDC
- 50090-7173
- 11-digit product format
- 500907173
- Labeler code
- 50090
- Product ID
- 50090-7173_5839c766-0032-4869-9c92-60531bcb183f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUDESONIDE
- Dosage form
- INHALANT
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- ANDA078202
- Marketing category
- ANDA
- Marketing start
- 2013-10-01
- 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 |
|---|
| 50090-7173-0 | 50090717300 | 30 AMPULE in 1 CARTON (50090-7173-0) / 2 mL in 1 AMPULE | 30 ampule | 2024-05-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Budesonide | A-S Medication Solutions | 2024-05-23 | HUMAN PRESCRIPTION DRUG LABEL | 2 |