Naproxen
- Product NDC
- 68788-6322
- 11-digit product format
- 687886322
- Labeler code
- 68788
- Product ID
- 68788-6322_6dd80b74-e1fc-4a90-a52c-ae09ee88d873
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091432
- Marketing category
- ANDA
- Marketing start
- 2016-10-10
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 500 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record