All Day Pain Relief
- Product NDC
- 0363-0169
- 11-digit product format
- 003630169
- Labeler code
- 0363
- Product ID
- 0363-0169_44d65894-b7e5-44d2-9238-c0ce93a7f61f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walgreens
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2014-03-31
- 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 |
|---|
| 0363-0169-01 | 00363016901 | 1 BOTTLE, PLASTIC in 1 BOX (0363-0169-01) > 100 TABLET in 1 BOTTLE, PLASTIC | 2014-03-31 | 2022-12-30 | No | No | Current |
| 0363-0169-24 | 00363016924 | 1 BOTTLE, PLASTIC in 1 BOX (0363-0169-24) > 24 TABLET in 1 BOTTLE, PLASTIC | 2014-03-31 | 2022-12-30 | No | No | Current |