Naproxen Sodium
- Product NDC
- 71335-0274
- 11-digit product format
- 713350274
- Labeler code
- 71335
- Product ID
- 71335-0274_9052d325-83d2-4ca0-aacc-fb1324742068
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2012-05-01
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0274-2 | 71335027402 | 20 TABLET in 1 BOTTLE (71335-0274-2) | 20 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-3 | 71335027403 | 30 TABLET in 1 BOTTLE (71335-0274-3) | 30 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-4 | 71335027404 | 40 TABLET in 1 BOTTLE (71335-0274-4) | 40 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-5 | 71335027405 | 50 TABLET in 1 BOTTLE (71335-0274-5) | 50 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-6 | 71335027406 | 60 TABLET in 1 BOTTLE (71335-0274-6) | 60 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-7 | 71335027407 | 14 TABLET in 1 BOTTLE (71335-0274-7) | 14 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-8 | 71335027408 | 100 TABLET in 1 BOTTLE (71335-0274-8) | 100 tablet | 2012-05-01 | 0000-00-00 | No | No | Current |
| 71335-0274-9 | 71335027409 | 90 TABLET in 1 BOTTLE (71335-0274-9) | 90 tablet | 2016-04-19 | 0000-00-00 | No | No | Current |