Oxaprozin
- Product NDC
- 63629-1345
- 11-digit product format
- 636291345
- Labeler code
- 63629
- Product ID
- 63629-1345_b7dfaeb7-b9d1-4242-a2f9-e756c5379436
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaprozin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-1345-1 | 63629134501 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1345-1) | 2009-12-09 | 0000-00-00 | No | No | Current |
| 63629-1345-2 | 63629134502 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-1345-2) | 2009-12-09 | 0000-00-00 | No | No | Current |
| 63629-1345-3 | 63629134503 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-1345-3) | 2022-02-08 | 0000-00-00 | No | No | Current |
| 63629-1345-4 | 63629134504 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-1345-4) | 2006-12-26 | 0000-00-00 | No | No | Current |
| 63629-1345-5 | 63629134505 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-1345-5) | 2009-05-20 | 0000-00-00 | No | No | Current |
| 63629-1345-6 | 63629134506 | 6 TABLET, FILM COATED in 1 BOTTLE (63629-1345-6) | 2022-02-08 | 0000-00-00 | No | No | Current |
| 63629-1345-7 | 63629134507 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-1345-7) | 2006-12-27 | 0000-00-00 | No | No | Current |