NDC 87063-292 – Nabumetone
Nabumetone 750 mg/1 · Tablet · Oral
Product NDC87063-292
Product details
- Brand name
- Nabumetone
- Generic name
- Nabumetone
- Labeler
- ASCLEMED USA INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078420
- Marketed since
- June 26, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Nabumetone 750 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 87063-292-01 | 100 TABLET in 1 BOTTLE (87063-292-01) | Aug 19, 2026 |
| 87063-292-06 | 6 TABLET in 1 BOTTLE (87063-292-06) | Aug 19, 2026 |
| 87063-292-07 | 7 TABLET in 1 BOTTLE (87063-292-07) | Aug 19, 2026 |
| 87063-292-10 | 10 TABLET in 1 BOTTLE (87063-292-10) | Aug 19, 2026 |
| 87063-292-20 | 20 TABLET in 1 BOTTLE (87063-292-20) | Aug 19, 2026 |
| 87063-292-30 | 30 TABLET in 1 BOTTLE (87063-292-30) | Aug 19, 2026 |
| 87063-292-60 | 60 TABLET in 1 BOTTLE (87063-292-60) | Aug 19, 2026 |
| 87063-292-90 | 90 TABLET in 1 BOTTLE (87063-292-90) | Aug 19, 2026 |
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