Naproxen Sodium
- Product NDC
- 57896-951
- 11-digit product format
- 578960951
- Labeler code
- 57896
- Product ID
- 57896-951_7c231a53-91a7-3ebc-e053-2a91aa0a4006
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceutical Corp
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2012-05-01
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record