All Day Pain Relief
- Product NDC
- 59726-023
- 11-digit product format
- 597260023
- Labeler code
- 59726
- Product ID
- 59726-023_4393d95e-758d-4f96-b672-59480fc0812c
- 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
- 2014-06-30
- Marketing end
- 2019-12-31
- 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