Oxaprozin
- Product NDC
- 55289-601
- 11-digit product format
- 552890601
- Labeler code
- 55289
- Product ID
- 55289-601_e236ae74-9277-32ce-e053-2995a90a6f00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaprozin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075849
- Marketing category
- ANDA
- Marketing start
- 2003-05-12
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-601-20 | 55289060120 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-601-20) | 2010-09-08 | 0000-00-00 | No | No | Current |
| 55289-601-30 | 55289060130 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-601-30) | 2010-09-08 | 0000-00-00 | No | No | Current |
| 55289-601-60 | 55289060160 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-601-60) | 2010-09-08 | 0000-00-00 | No | No | Current |