Budesonide
- Product NDC
- 51407-224
- 11-digit product format
- 514070224
- Labeler code
- 51407
- Product ID
- 51407-224_ac3b438c-bb10-249d-e053-2a95a90a9ddc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA205457
- Marketing category
- ANDA
- Marketing start
- 2018-07-03
- Marketing end
- 0000-00-00
- Substance
- BUDESONIDE
- Active strength
- 9 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51407-224-30 | 51407022430 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51407-224-30) | 2019-05-30 | 0000-00-00 | No | No | Current |