Budesonide
- Product NDC
- 51407-366
- 11-digit product format
- 514070366
- Labeler code
- 51407
- Product ID
- 51407-366_c8975701-4160-1019-e053-2995a90a18d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA208851
- Marketing category
- ANDA
- Marketing start
- 2020-09-17
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-366 | BUDESONIDE TABLET, FILM COATED, EXTENDED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 2 | Legacy NDC | 20250101_c8975701-419c-1019-e053-2995a90a18d8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-366-30 | 51407036630 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-366-30) | 2020-11-03 | 0000-00-00 | No | No | Current |