All Day Pain Relief
- Product NDC
- 41163-167
- 11-digit product format
- 411630167
- Labeler code
- 41163
- Product ID
- 41163-167_58de8f2d-ff20-4445-865a-8c4ae15e6711
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EQUALINE (SuperValu)
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2013-05-09
- Marketing end
- 2020-05-09
- 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