All Day Pain Relief
- Product NDC
- 59726-256
- 11-digit product format
- 597260256
- Labeler code
- 59726
- Product ID
- 59726-256_eef8b012-dd93-4d27-9b3d-7be965d7c8da
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2014-03-28
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-256-15 | 59726025615 | 1 BOTTLE, PLASTIC in 1 BOX (59726-256-15) > 15 TABLET in 1 BOTTLE, PLASTIC | 2014-03-28 | 0000-00-00 | No | No | Current |