NDC 71335-0617 – Oxaprozin
Oxaprozin 600 mg/1 · Tablet · Oral
Product NDC71335-0617
Product details
- Brand name
- Oxaprozin
- Generic name
- Oxaprozin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208633
- Marketed since
- May 4, 2017
- 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 |
|---|---|---|
| 71335-0617-1 | 30 TABLET in 1 BOTTLE (71335-0617-1) | Dec 27, 2021 |
| 71335-0617-2 | 20 TABLET in 1 BOTTLE (71335-0617-2) | Dec 27, 2021 |
| 71335-0617-3 | 14 TABLET in 1 BOTTLE (71335-0617-3) | Dec 27, 2021 |
| 71335-0617-4 | 60 TABLET in 1 BOTTLE (71335-0617-4) | Feb 14, 2018 |
| 71335-0617-5 | 90 TABLET in 1 BOTTLE (71335-0617-5) | Apr 5, 2018 |
| 71335-0617-6 | 6 TABLET in 1 BOTTLE (71335-0617-6) | Dec 27, 2021 |
| 71335-0617-7 | 120 TABLET in 1 BOTTLE (71335-0617-7) | Dec 27, 2021 |
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- 71335-0393 Oxaprozin 600 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 72189-595 Oxaprozin 600 mg/1 · Tablet, Film Coated · Direct_Rx
- 55111-170 Oxaprozin 600 mg/1 · Tablet, Film Coated · Dr. Reddy's Laboratories Limited
- 82804-261 Oxaprozin 600 mg/1 · Tablet, Film Coated · Proficient Rx LP
- 70512-787 Oxaprozin 300 mg/1 · Capsule · SOLA Pharmaceuticals, LLC
- 60760-382 Oxaprozin 600 mg/1 · Tablet, Film Coated · ST MARY'S MEDICAL PARK PHARMACY