NDC 62207-762 – Naproxen Sodium
Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral
Product NDC62207-762
Product details
- Brand name
- Naproxen Sodium
- Generic name
- Naproxen Sodium
- Labeler
- Granules India Ltd
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091353
- Marketed since
- September 30, 2011
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 62207-762-42 | 50 TABLET, FILM COATED in 1 BOTTLE (62207-762-42) | Sep 30, 2011 |
| 62207-762-43 | 100 TABLET, FILM COATED in 1 BOTTLE (62207-762-43) | Sep 30, 2011 |
| 62207-762-47 | 500 TABLET, FILM COATED in 1 BOTTLE (62207-762-47) | Sep 30, 2011 |
| 62207-762-49 | 1000 TABLET, FILM COATED in 1 BOTTLE (62207-762-49) | Sep 30, 2011 |
Recalls mentioning this NDC
- D-0777-2021 Sep 8, 2021 · Class II
CGMP Deviations
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