Naproxen
- Product NDC
- 70518-1408
- 11-digit product format
- 705181408
- Labeler code
- 70518
- Product ID
- 70518-1408_b8df8259-aec9-dee4-e053-2995a90aa87b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091432
- Marketing category
- ANDA
- Marketing start
- 2018-09-11
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1408-0 | 70518140800 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1408-0) | 2018-09-11 | 0000-00-00 | No | No | Current |