All Day Pain Relief
- Product NDC
- 41163-169
- 11-digit product format
- 411630169
- Labeler code
- 41163
- Product ID
- 41163-169_ed62cc13-c025-444a-a866-2152c984b9f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EQUALINE (SuperValu)
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2010-11-15
- Marketing end
- 2020-11-15
- 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