NDC 71205-030 – Nabumetone
Nabumetone 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-030
Product details
- Brand name
- Nabumetone
- Generic name
- Nabumetone
- Labeler
- Proficient Rx LP
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-030-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-20) | Jan 19, 2022 |
| 71205-030-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-30) | May 1, 2018 |
| 71205-030-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-60) | May 1, 2018 |
| 71205-030-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-90) | May 1, 2018 |
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