Composition
- Active ingredients
- NABUMETONE 750MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NABUMETONE 500MG · TabletANDA078420-001 · Prescription
- NABUMETONE 750MG · TabletANDA078420-002 · Prescription
- NABUMETONE 500MG · TabletANDA075590-001 · Discontinued
- NABUMETONE 750MG · TabletANDA075590-002 · Discontinued
- NABUMETONE 500MG · TabletANDA090427-001 · Discontinued
- NABUMETONE 750MG · TabletANDA090427-002 · Discontinued
- NABUMETONE 750MG · TabletANDA075179-001 · Discontinued
- NABUMETONE 500MG · TabletANDA078671-001 · Prescription
- NABUMETONE 750MG · TabletANDA078671-002 · Prescription
- NABUMETONE 500MG · TabletANDA091083-001 · Prescription
- NABUMETONE 750MG · TabletANDA091083-002 · Prescription
- NABUMETONE 750MG · TabletANDA203166-002 · Prescription
- NABUMETONE 1GM · TabletANDA203166-003 · Prescription
- NABUMETONE 500MG · Tablet
At a glance
- Brand name
- Nabumetone
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Impax Labs Inc
- Status
- Discontinued
- FDA approval
- 26 May 2000
- Application
- ANDA075189-002