Daypro
- Product NDC
- 55289-453
- 11-digit product format
- 552890453
- Labeler code
- 55289
- Product ID
- 55289-453_d9f63229-62c8-3853-e053-2995a90a63c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxaprozin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA018841
- Marketing category
- NDA
- Marketing start
- 1992-10-29
- 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 |
|---|
| 55289-453-14 | 55289045314 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-14) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-15 | 55289045315 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-15) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-20 | 55289045320 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-20) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-30 | 55289045330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-30) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-40 | 55289045340 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-40) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-42 | 55289045342 | 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-42) | 2010-04-14 | 0000-00-00 | No | No | Current |
| 55289-453-60 | 55289045360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-60) | 2010-04-14 | 0000-00-00 | No | No | Current |