All Day Pain Relief
- Product NDC
- 55315-168
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Freds Inc
- 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 |
|---|
| 55315-168-01 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-01) > 100 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | Current |
| 55315-168-24 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-24) > 24 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | Current |
| 55315-168-50 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-50) > 50 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | Current |