All Day Pain Relief
- Product NDC
- 0363-0169
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walgreens
- Application
- ANDA079096
- Marketing category
- ANDA
- Substance
- NAPROXEN SODIUM
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0363-0169-01 | 1 BOTTLE, PLASTIC in 1 BOX (0363-0169-01) > 100 TABLET in 1 BOTTLE, PLASTIC | 2014-03-31 | 2022-12-30 | No | Current |
| 0363-0169-24 | 1 BOTTLE, PLASTIC in 1 BOX (0363-0169-24) > 24 TABLET in 1 BOTTLE, PLASTIC | 2014-03-31 | 2022-12-30 | No | Current |