Naproxen Sodium 71335-1061
Product NDC
71335-1061- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- April 11, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA074661
Active Ingredients
| Ingredient | Strength |
|---|---|
| Naproxen Sodium | 220 mg/1 |
Drug Class
Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]
Packaging Options(8)
20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1061-2)
40 TABLET, FILM COATED in 1 BOTTLE (71335-1061-3)
50 TABLET, FILM COATED in 1 BOTTLE (71335-1061-4)
60 TABLET, FILM COATED in 1 BOTTLE (71335-1061-5)
14 TABLET, FILM COATED in 1 BOTTLE (71335-1061-6)
100 TABLET, FILM COATED in 1 BOTTLE (71335-1061-7)
90 TABLET, FILM COATED in 1 BOTTLE (71335-1061-8)