All Day Relief
- Product NDC
- 68788-9971
- 11-digit product format
- 687889971
- Labeler code
- 68788
- Product ID
- 68788-9971_37495b5f-dbb5-4163-b340-2b45fe4e6da6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium Tablet, coated
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2015-05-06
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record