NDC 71335-0393 – Oxaprozin
Oxaprozin 600 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0393
Product details
- Brand name
- Oxaprozin
- Generic name
- Oxaprozin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075855
- Marketed since
- January 31, 2001
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Oxaprozin 600 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0393-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1) | Sep 12, 2007 |
| 71335-0393-2 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2) | Sep 12, 2007 |
| 71335-0393-3 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3) | Sep 12, 2007 |
| 71335-0393-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4) | Sep 12, 2007 |
| 71335-0393-5 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5) | Sep 12, 2007 |
| 71335-0393-6 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6) | Sep 12, 2007 |
| 71335-0393-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7) | Sep 12, 2007 |
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