NDC 63941-144 – All Day Pain Relief
Naproxen Sodium 220 mg/1 · Tablet, Coated · Oral
Product NDC63941-144
Product details
- Brand name
- All Day Pain Relief
- Generic name
- Naproxen Sodium
- Labeler
- VALU MERCHANDISERS COMPANY
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA079096
- Marketed since
- June 10, 2010
- Marketing end
- October 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Naproxen Sodium 220 mg/1
Uses, dosage, side effects and warnings for All Day Pain Relief →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63941-144-01 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC | Jun 29, 2010 |
| 63941-144-02 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC | Jun 10, 2010 |
| 63941-144-03 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC | Aug 3, 2010 |
Other All Day Pain Relief products
- 63941-245 Naproxen Sodium 220 mg/1 · Tablet, Coated · VALU MERCHANDISERS COMPANY
- 0363-6099 Naproxen Sodium 220 mg/1 · Tablet, Coated · WALGREENS
- 0363-9608 Naproxen Sodium 220 mg/1 · Tablet, Coated · WALGREENS
- 37808-068 Naproxen Sodium 220 mg/1 · Tablet · H E B
- 69517-109 Naproxen Sodium 220 mg/1 · Tablet · HealthLife of USA LLC
- 0363-0368 Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Walgreen Company
- 0363-0938 Naproxen Sodium 200 mg/1 · Tablet, Film Coated · Walgreen Company
- 79903-005 Naproxen Sodium 220 mg/1 · Tablet, Film Coated · WALMART INC.
- 79903-389 Naproxen Sodium 220 mg/1 · Tablet · Walmart Inc.