members mark naproxen sodium
- Product NDC
- 68196-368
- 11-digit product format
- 681960368
- Labeler code
- 68196
- Product ID
- 68196-368_a9d57247-5fca-4414-b7a9-4de832187c2a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sam's West Inc
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2007-05-29
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68196-368 | MEMBERS MARK NAPROXEN SODIUM (NAPROXEN SODIUM) TABLET, FILM COATED [SAM'S WEST INC] | 7 | Legacy NDC | 20211130_40a53cbf-93e9-46cb-a2bb-dc6911a56c6c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68196-368-79 | 68196036879 | 400 TABLET, FILM COATED in 1 BOTTLE (68196-368-79) | 2009-03-08 | 0000-00-00 | No | No | Current |