All Day Pain Relief
- Product NDC
- 15127-168
- 11-digit product format
- 151270168
- Labeler code
- 15127
- Product ID
- 15127-168_02a53e68-fa20-43c9-a339-fba9f4b20c4f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Select Brand Dist.
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2016-06-30
- 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 |
|---|
| 15127-168-24 | 15127016824 | 1 BOTTLE, PLASTIC in 1 BOX (15127-168-24) > 24 TABLET in 1 BOTTLE, PLASTIC | 2016-06-30 | 2022-12-30 | No | No | Current |