NDC 69230-329 – Naproxen sodium
Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC69230-329
Product details
- Brand name
- Naproxen sodium
- Generic name
- Naproxen sodium
- Labeler
- Camber Consumer Care Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211065
- Marketed since
- October 28, 2022
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 69230-329-01 | 1 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLE | Oct 28, 2022 |
| 69230-329-02 | 1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLE | Oct 28, 2022 |
| 69230-329-05 | 500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05) | Oct 28, 2022 |
| 69230-329-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10) | Oct 28, 2022 |
| 69230-329-24 | 1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLE | Oct 28, 2022 |
| 69230-329-50 | 1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE | Oct 28, 2022 |
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