Naproxen Sodium
- Product NDC
- 71800-020
- 11-digit product format
- 718000020
- Labeler code
- 71800
- Product ID
- 71800-020_eea86dc6-400b-428a-9d49-20893bcd54b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Innovida Phamaceutique Corporation
- Application
- NDA020353
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-02-07
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 375 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record