NDC 71335-1061 – Naproxen Sodium
Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1061
Product details
- Brand name
- Naproxen Sodium
- Generic name
- Naproxen Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA074661
- Marketed since
- April 11, 2014
- Listing expires
- December 31, 2026
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1061-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1) | Dec 28, 2021 |
| 71335-1061-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1061-2) | Jan 16, 2019 |
| 71335-1061-3 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-1061-3) | Dec 28, 2021 |
| 71335-1061-4 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-1061-4) | Dec 28, 2021 |
| 71335-1061-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1061-5) | Dec 28, 2021 |
| 71335-1061-6 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1061-6) | Dec 28, 2021 |
| 71335-1061-7 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1061-7) | Dec 28, 2021 |
| 71335-1061-8 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1061-8) | Dec 28, 2021 |
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