NDC 71335-0822 – Naproxen Sodium
Naproxen Sodium 550 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0822
Product details
- Brand name
- Naproxen Sodium
- Generic name
- Naproxen Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200629
- Marketed since
- October 31, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Naproxen Sodium 550 mg/1
Uses, dosage, side effects and warnings for Naproxen Sodium →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0822-0 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-0822-0) | Jan 29, 2025 |
| 71335-0822-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0822-1) | Feb 21, 2020 |
| 71335-0822-2 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0822-2) | Jan 29, 2025 |
| 71335-0822-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0822-3) | Aug 23, 2018 |
| 71335-0822-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-4) | May 29, 2018 |
| 71335-0822-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0822-5) | Apr 26, 2018 |
| 71335-0822-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0822-6) | Jan 29, 2025 |
| 71335-0822-7 | 42 TABLET, FILM COATED in 1 BOTTLE (71335-0822-7) | Jan 29, 2025 |
| 71335-0822-8 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0822-8) | Jan 29, 2025 |
| 71335-0822-9 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-0822-9) | Jan 29, 2025 |
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