All Day
- Product NDC
- 49781-101
- 11-digit product format
- 497810101
- Labeler code
- 49781
- Product ID
- 49781-101_4c952477-9cdb-4aa5-9547-7a3e99b9c15c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health (Leader) 49781
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2014-07-31
- Marketing end
- 2020-07-31
- 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