NDC 0591-2510 – Budesonide
Budesonide 9 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0591-2510
Product details
- Brand name
- Budesonide
- Generic name
- Budesonide
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205457
- Marketed since
- July 5, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Budesonide 9 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0591-2510-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2510-30) | Jul 5, 2018 |
Recalls mentioning this NDC
- D-0275-2024 Feb 7, 2024 · Class II
Failed Dissolution Specifications
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