NDC 71335-1234 – Nabumetone
Nabumetone 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1234
Product details
- Brand name
- Nabumetone
- Generic name
- Nabumetone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091083
- Marketed since
- June 13, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Nabumetone 500 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1234-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1234-1) | May 29, 2019 |
| 71335-1234-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1234-2) | Oct 22, 2019 |
| 71335-1234-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1234-3) | Jul 3, 2019 |
| 71335-1234-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1234-4) | Jun 19, 2019 |
| 71335-1234-5 | 42 TABLET, FILM COATED in 1 BOTTLE (71335-1234-5) | May 2, 2022 |
| 71335-1234-6 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-1234-6) | Jul 15, 2019 |
| 71335-1234-7 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1234-7) | May 2, 2022 |
| 71335-1234-8 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1234-8) | May 2, 2022 |
| 71335-1234-9 | 9 TABLET, FILM COATED in 1 BOTTLE (71335-1234-9) | May 2, 2022 |
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