Naproxen Sodium
- Product NDC
- 41250-073
- 11-digit product format
- 412500073
- Labeler code
- 41250
- Product ID
- 41250-073_1ab1e8f9-e364-4220-b1f7-8a531d931b1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- NDA021920
- Marketing category
- NDA
- Marketing start
- 2014-09-30
- Marketing end
- 2024-04-26
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 41250-073-40 | 41250007340 | 1 BOTTLE, PLASTIC in 1 BOX (41250-073-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-09-30 | 2024-04-26 | No | No | Current |
| 41250-073-80 | 41250007380 | 1 BOTTLE, PLASTIC in 1 BOX (41250-073-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-09-30 | 2024-04-26 | No | No | Current |