Naproxen
- Product NDC
- 71205-469
- 11-digit product format
- 712050469
- Labeler code
- 71205
- Product ID
- 71205-469_cb2a9c90-6e47-41b2-b630-430bddcec7ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075227
- Marketing category
- ANDA
- Marketing start
- 1998-07-31
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 375 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71205-469-30 | 71205046930 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-30) | 2020-08-14 | 0000-00-00 | No | No | Current |
| 71205-469-60 | 71205046960 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-60) | 2020-08-14 | 0000-00-00 | No | No | Current |
| 71205-469-90 | 71205046990 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-469-90) | 2020-08-14 | 0000-00-00 | No | No | Current |