Naproxen
- Product NDC
- 70868-200
- 11-digit product format
- 708680200
- Labeler code
- 70868
- Product ID
- 70868-200_ee815be2-8c61-41de-8397-72a0d1908be5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Key Therapeutics, LLC
- Application
- NDA018965
- Marketing category
- NDA
- Marketing start
- 2016-11-11
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 125 mg/5mL
- 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