NDC 55111-170 – Oxaprozin
Oxaprozin 600 mg/1 · Tablet, Film Coated · Oral
Product NDC55111-170
Product details
- Brand name
- Oxaprozin
- Generic name
- Oxaprozin
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075855
- Marketed since
- January 31, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Oxaprozin 600 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 55111-170-01 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-170-01) | Jan 31, 2001 |
| 55111-170-05 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-170-05) | Jan 31, 2001 |
Other Oxaprozin products
- 71335-0393 Oxaprozin 600 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 72189-595 Oxaprozin 600 mg/1 · Tablet, Film Coated · Direct_Rx
- 82804-261 Oxaprozin 600 mg/1 · Tablet, Film Coated · Proficient Rx LP
- 60760-382 Oxaprozin 600 mg/1 · Tablet, Film Coated · ST MARY'S MEDICAL PARK PHARMACY
- 69238-1120 Oxaprozin 600 mg/1 · Tablet · Amneal Pharmaceuticals NY LLC
- 71335-0617 Oxaprozin 600 mg/1 · Tablet · Bryant Ranch Prepack
- 62135-176 Oxaprozin 600 mg/1 · Tablet · Chartwell RX, LLC.
- 70512-787 Oxaprozin 300 mg/1 · Capsule · SOLA Pharmaceuticals, LLC