Oxaprozin
- Product NDC
- 63629-8724
- 11-digit product format
- 636298724
- Labeler code
- 63629
- Product ID
- 63629-8724_1dc2d61f-6958-4e0c-b4b4-ae659eb86e83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaprozin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075845
- Marketing category
- ANDA
- Marketing start
- 2001-01-31
- Substance
- OXAPROZIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MHJ80W9LRB | OXAPROZIN | 21256-18-8 | OXAPROZIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-8724-1 | 63629872401 | 100 TABLET in 1 BOTTLE (63629-8724-1) | 100 tablet | 2021-08-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oxaprozin | Bryant Ranch Prepack | 2023-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 103 |