Naproxen Sodium
- Product NDC
- 41163-174
- 11-digit product format
- 411630174
- Labeler code
- 41163
- Product ID
- 41163-174_e3c39bae-648e-417e-97b9-465b71479272
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- EQUALINE (SuperValu)
- Application
- NDA021920
- Marketing category
- NDA
- Marketing start
- 2014-09-30
- Marketing end
- 2021-12-30
- 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 |
|---|
| 41163-174-20 | 41163017420 | 1 BOTTLE, PLASTIC in 1 BOX (41163-174-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-09-30 | 2021-12-30 | No | No | Current |
| 41163-174-40 | 41163017440 | 1 BOTTLE, PLASTIC in 1 BOX (41163-174-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-09-30 | 2021-12-30 | No | No | Current |
| 41163-174-80 | 41163017480 | 1 BOTTLE, PLASTIC in 1 BOX (41163-174-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-09-30 | 2021-12-30 | No | No | Current |