All Day Pain Relief
- Product NDC
- 30142-168
- 11-digit product format
- 301420168
- Labeler code
- 30142
- Product ID
- 30142-168_8ff9a2e3-ee93-4424-b4be-68ea06012f0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Kroger Co.
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2011-02-02
- 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