Naproxen Sodium 50844-0417
Product NDC
50844-0417- Manufacturer
- L.n.k. International, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 1, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA204872
Active Ingredients
| Ingredient | Strength |
|---|---|
| Naproxen Sodium | 220 mg/1 |
Drug Class
Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]
Packaging Options(8)
60 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)
1 BOTTLE, PLASTIC in 1 CARTON (50844-417-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
48 POUCH in 1 CARTON (50844-417-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)
8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)
8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)