Composition
- Active ingredients
- OXAPROZIN 600MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- OXAPROZIN 600MG · TabletANDA075849-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075855-001 · Prescription
- OXAPROZIN 600MG · TabletANDA208633-001 · Prescription
- OXAPROZIN 600MG · TabletANDA075848-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075850-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075846-001 · Discontinued
- OXAPROZIN 600MG · TabletThis page
- OXAPROZIN 600MG · TabletANDA075987-001 · Prescription
- OXAPROZIN 600MG · TabletANDA075842-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075843-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075845-001 · Prescription
- OXAPROZIN 600MG · TabletANDA075844-001 · Discontinued
- OXAPROZIN 600MG · TabletANDA075847-001 · Discontinued
Official product information
At a glance
- Brand name
- Oxaprozin
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Pharmobedient
- Status
- Discontinued
- FDA approval
- 17 Aug 2001
- Application
- ANDA075851-001