oxaprozin
- Product NDC
- 59762-6002
- 11-digit product format
- 597626002
- Labeler code
- 59762
- Product ID
- 59762-6002_fcadb9d0-958e-4d05-97a7-5b18dbf6e230
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxaprozin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA018841
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-03-27
- 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 |
|---|
| 59762-6002-1 | 59762600201 | 100 TABLET, FILM COATED in 1 BOTTLE (59762-6002-1) | 2013-03-27 | 0000-00-00 | No | No | Current |