Naproxen Sodium 220mg
- Product NDC
- 53329-678
- 11-digit product format
- 533290678
- Labeler code
- 53329
- Product ID
- 53329-678_d0fe95b4-fcd3-05eb-e053-2995a90a0596
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medline Industries, LP
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2018-03-07
- Marketing end
- 2022-05-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53329-678-30 | 53329067830 | 100 TABLET in 1 BOTTLE (53329-678-30) | 100 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |