Budesonide
- Product NDC
- 21130-710
- 11-digit product format
- 211300710
- Labeler code
- 21130
- Product ID
- 21130-710_e992feff-005d-8eaf-dd5c-f1189e69b4ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Safeway
- Application
- ANDA078949
- Marketing category
- ANDA
- Marketing start
- 2016-09-15
- Marketing end
- 2023-10-24
- Substance
- BUDESONIDE
- Active strength
- 32 ug/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-710-06 | 21130071006 | 1 BOTTLE, SPRAY in 1 BOTTLE, SPRAY (21130-710-06) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY | 2016-09-15 | 0000-00-00 | No | No | Current |