All Day Pain Relief
- Product NDC
- 55315-168
- 11-digit product format
- 553150168
- Labeler code
- 55315
- Product ID
- 55315-168_e5bad7e7-9289-40d3-abca-afa22a5bfb76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Freds Inc
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2015-09-30
- Marketing end
- 2024-04-26
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55315-168-01 | 55315016801 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-01) > 100 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | No | Current |
| 55315-168-24 | 55315016824 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-24) > 24 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | No | Current |
| 55315-168-50 | 55315016850 | 1 BOTTLE, PLASTIC in 1 BOX (55315-168-50) > 50 TABLET in 1 BOTTLE, PLASTIC | 2015-09-30 | 2024-04-26 | No | No | Current |