Budesonide
- Product NDC
- 50090-6586
- 11-digit product format
- 500906586
- Labeler code
- 50090
- Product ID
- 50090-6586_6cd18e8a-1a34-4e9e-914c-198ef79a8a83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- SUSPENSION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- ANDA211922
- Marketing category
- ANDA
- Marketing start
- 2021-05-01
- Substance
- BUDESONIDE
- Active strength
- .5 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Budesonide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUDESONIDE | .5 mg/2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q3OKS62Q6X |
| Rxcui | 351109 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6586-0 | Budesonide | 6 in 1 CARTON | SUSPENSION | 6 | | 3 |
| 50090-6586-0 | Budesonide | 5 in 1 POUCH | SUSPENSION | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6586 | BUDESONIDE SUSPENSION [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, 2 package rows | 20250223_4a7d97e0-36f7-4ac9-8f9b-4c3aac568c2b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6586-0 | 50090658600 | 6 POUCH in 1 CARTON (50090-6586-0) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE | 6 pouch | 2023-08-09 | No | No | Historical |