NDC 58602-819 – Naproxen Sodium
Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC58602-819
Product details
- Brand name
- Naproxen Sodium
- Generic name
- Naproxen Sodium
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205497
- Marketed since
- December 11, 2017
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 58602-819-07 | 1 BOTTLE in 1 CARTON (58602-819-07) / 24 TABLET, FILM COATED in 1 BOTTLE | Oct 25, 2021 |
| 58602-819-14 | 1 BOTTLE in 1 CARTON (58602-819-14) / 50 TABLET, FILM COATED in 1 BOTTLE | Dec 11, 2017 |
| 58602-819-19 | 1 BOTTLE in 1 CARTON (58602-819-19) / 90 TABLET, FILM COATED in 1 BOTTLE | Sep 21, 2023 |
| 58602-819-21 | 1 BOTTLE in 1 CARTON (58602-819-21) / 100 TABLET, FILM COATED in 1 BOTTLE | Dec 11, 2017 |
| 58602-819-29 | 1 BOTTLE in 1 CARTON (58602-819-29) / 150 TABLET, FILM COATED in 1 BOTTLE | Oct 25, 2021 |
| 58602-819-38 | 1 BOTTLE in 1 CARTON (58602-819-38) / 300 TABLET, FILM COATED in 1 BOTTLE | Oct 25, 2021 |
| 58602-819-40 | 1 BOTTLE in 1 CARTON (58602-819-40) / 500 TABLET, FILM COATED in 1 BOTTLE | Oct 25, 2021 |
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