Naproxen
- Product NDC
- 69168-361
- 11-digit product format
- 691680361
- Labeler code
- 69168
- Product ID
- 69168-361_1b97ae91-7304-49f3-a5aa-38973bb61c49
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium 220 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Allegiant Health
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2014-12-23
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69168-361 | NAPROXEN ALL DAY RELIEF FOR PAIN (NAPROXEN SODIUM 220 MG) TABLET [ALLEGIANT HEALTH] | 1 | Legacy NDC | 20141224_1b97ae91-7304-49f3-a5aa-38973bb61c49.zip |