Naproxen Sodium
- Product NDC
- 68071-2333
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA212199
- Marketing category
- ANDA
- Substance
- NAPROXEN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-2333-2 | 21 TABLET in 1 BOTTLE (68071-2333-2) | 2024-12-19 | | No | Historical |
| 68071-2333-3 | 30 TABLET in 1 BOTTLE (68071-2333-3) | 2021-01-14 | | No | Historical |
| 68071-2333-4 | 14 TABLET in 1 BOTTLE (68071-2333-4) | 2021-01-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Naproxen Sodium | NuCare Pharmaceuticals,Inc. | 2025-01-03 | HUMAN PRESCRIPTION DRUG LABEL | 3 |