Naproxen Sodium
- Product NDC
- 59726-748
- 11-digit product format
- 597260748
- Labeler code
- 59726
- Product ID
- 59726-748_91614b04-3c7c-4b34-9cea-46165ea3ef75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA208363
- Marketing category
- ANDA
- Marketing start
- 2022-02-25
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-748 | NAPROXEN SODIUM CAPSULE, LIQUID FILLED [P & L DEVELOPMENT, LLC] | 4 | Legacy NDC | 20241106_82ffcc82-1bcf-4c2b-92d2-fe273ebe5cab.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-748-20 | 59726074820 | 1 BOTTLE, PLASTIC in 1 BOX (59726-748-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2022-02-25 | 0000-00-00 | No | No | Current |
| 59726-748-80 | 59726074880 | 1 BOTTLE, PLASTIC in 1 BOX (59726-748-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2022-02-25 | 0000-00-00 | No | No | Current |