NDC 71335-1272 – Nabumetone
Nabumetone 750 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1272
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 750 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1272-0 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1272-0) | Jun 29, 2022 |
| 71335-1272-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1272-1) | Jul 16, 2019 |
| 71335-1272-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1272-2) | Jun 29, 2022 |
| 71335-1272-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1272-3) | Jul 17, 2019 |
| 71335-1272-4 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1272-4) | Jun 29, 2022 |
| 71335-1272-5 | 42 TABLET, FILM COATED in 1 BOTTLE (71335-1272-5) | Jun 29, 2022 |
| 71335-1272-6 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1272-6) | Jun 29, 2022 |
| 71335-1272-7 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1272-7) | Jun 29, 2022 |
| 71335-1272-8 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-1272-8) | Jun 29, 2022 |
| 71335-1272-9 | 9 TABLET, FILM COATED in 1 BOTTLE (71335-1272-9) | Jun 29, 2022 |
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