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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Budesonide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUDESONIDE | .25 mg/2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q3OKS62Q6X |
| Rxcui | 349094 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7173-0 | Budesonide | 30 in 1 CARTON | INHALANT | 30 | | 2 |
| 50090-7173-0 | Budesonide | 2 mL in 1 AMPULE | INHALANT | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7173 | BUDESONIDE INHALANT [A-S MEDICATION SOLUTIONS] | 2 | Current NDC, 2 package rows | 20240524_521a79d0-4d93-45f7-8feb-8d2b502dd216.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 |
|---|
| 50090-7173-0 | 50090717300 | 30 AMPULE in 1 CARTON (50090-7173-0) / 2 mL in 1 AMPULE | 30 ampule | 2024-05-21 | No | No | Current |