All Day Pain Relief
- Product NDC
- 59779-172
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA079096
- Marketing category
- ANDA
- Substance
- NAPROXEN SODIUM
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
No records found.