NDC 47335-722 – Febuxostat
Febuxostat 80 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-722
Product details
- Brand name
- Febuxostat
- Generic name
- Febuxostat
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205467
- Marketed since
- July 5, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Febuxostat 80 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 47335-722-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-722-18) | Jul 5, 2019 |
| 47335-722-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-722-83) | Jul 5, 2019 |
| 47335-722-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-722-88) | Jul 5, 2019 |
Recalls mentioning this NDC
- D-0265-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment. - D-0264-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
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