Budesonide
- Product NDC
- 69842-001
- 11-digit product format
- 698420001
- Labeler code
- 69842
- Product ID
- 69842-001_e78eb875-a802-43b8-8672-cbde17e9b607
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- CVS Pharmacy
- Application
- ANDA078949
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- BUDESONIDE
- Active strength
- 32 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Budesonide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUDESONIDE | 32 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q3OKS62Q6X |
| Rxcui | 1797929 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69842-001-01 | Budesonide | 1 in 1 BOTTLE, SPRAY | SPRAY, METERED | 1 | | 10 |
| 69842-001-01 | Budesonide | 120 in 1 BOTTLE, SPRAY | SPRAY, METERED | 120 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-001 | BUDESONIDE SPRAY, METERED [CVS PHARMACY] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241004_b2650d29-c011-48f1-a7f4-040011d4563d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-001-01 | 69842000101 | 1 BOTTLE, SPRAY in 1 BOTTLE, SPRAY (69842-001-01) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY | 2025-07-01 | 0000-00-00 | No | No | Current |