All Day Pain Relief
- Product NDC
- 49781-146
- 11-digit product format
- 497810146
- Labeler code
- 49781
- Product ID
- 49781-146_62668453-97a0-469e-bad4-a52f59a28575
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health (Leader) 49781
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2015-11-30
- Marketing end
- 2022-02-01
- 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 |
|---|
| 49781-146-50 | 49781014650 | 1 BOTTLE, PLASTIC in 1 BOX (49781-146-50) > 50 TABLET in 1 BOTTLE, PLASTIC | 2015-11-30 | 2022-02-01 | No | No | Current |
| 49781-146-51 | 49781014651 | 1 BOTTLE, PLASTIC in 1 BOX (49781-146-51) > 100 TABLET in 1 BOTTLE, PLASTIC | 2015-11-30 | 2022-02-01 | No | No | Current |