Sumatriptan And Naproxen Sodium 47335-0410
Product NDC
47335-0410- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 20, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA202803
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naproxen Sodium | 500 mg/1 |
| Sumatriptan Succinate | 85 mg/1 |
Drug Class
Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]
Packaging Options(3)
9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22)
30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83)
100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)