Naproxen Sodium
- Product NDC
- 11673-175
- 11-digit product format
- 116730175
- Labeler code
- 11673
- Product ID
- 11673-175_867ec93b-5f0e-49fd-b463-e8eabb512c56
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- NDA021920
- Marketing category
- NDA
- Marketing start
- 2014-12-30
- Marketing end
- 2022-12-30
- 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 |
|---|
| 11673-175-18 | 11673017518 | 180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11673-175-18) | 2014-12-30 | 2022-12-30 | No | No | Current |
| 11673-175-40 | 11673017540 | 1 BOTTLE, PLASTIC in 1 BOX (11673-175-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-12-30 | 2022-12-30 | No | No | Current |
| 11673-175-80 | 11673017580 | 1 BOTTLE, PLASTIC in 1 BOX (11673-175-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2014-12-30 | 2022-12-30 | No | No | Current |