Naproxen Sodium
- Product NDC
- 0480-0953
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naproxen sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA075416
- Marketing category
- ANDA
- Substance
- NAPROXEN SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0480-0953-56 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0480-0953-56) | 2022-11-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Naproxen Sodium | Teva Pharmaceuticals, Inc. | 2024-12-30 | HUMAN PRESCRIPTION DRUG LABEL | 6 |