NDC 37808-713 – Naproxen sodium
Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC37808-713
Product details
- Brand name
- Naproxen sodium
- Generic name
- Naproxen Sodium
- Labeler
- H E B
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA074661
- Marketed since
- October 3, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Naproxen Sodium 220 mg/1
Uses, dosage, side effects and warnings for Naproxen Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 37808-713-62 | 1 BOTTLE in 1 CARTON (37808-713-62) / 24 TABLET, FILM COATED in 1 BOTTLE (37808-713-24) | Jun 19, 2026 |
| 37808-713-71 | 1 BOTTLE in 1 CARTON (37808-713-71) / 50 TABLET, FILM COATED in 1 BOTTLE (37808-713-50) | Jun 19, 2026 |
| 37808-713-75 | 1 BOTTLE in 1 CARTON (37808-713-75) / 90 TABLET, FILM COATED in 1 BOTTLE (37808-713-90) | Jun 19, 2026 |
| 37808-713-79 | 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79) | Oct 3, 2017 |
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