NDC 47335-410 – Sumatriptan and Naproxen Sodium
Sumatriptan Succinate 85 mg/1; Naproxen Sodium 500 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-410
Product details
- Brand name
- Sumatriptan and Naproxen Sodium
- Generic name
- Sumatriptan and Naproxen Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202803
- Marketed since
- July 20, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug; Serotonin-1b and Serotonin-1d Receptor Agonist
Active ingredients
- Sumatriptan Succinate 85 mg/1
- Naproxen Sodium 500 mg/1
Uses, dosage, side effects and warnings for Sumatriptan and Naproxen Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 47335-410-22 | 9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22) | Jul 20, 2018 |
| 47335-410-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83) | Jul 20, 2018 |
| 47335-410-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88) | Jul 20, 2018 |