Naproxen Sodium
- Product NDC
- 63940-763
- 11-digit product format
- 639400763
- Labeler code
- 63940
- Product ID
- 63940-763_99eb0620-baf1-5fa1-e053-2a95a90a03d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HARMON STORES INC.
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63940-763-05 | Naproxen Sodium | 50 in 1 BOTTLE | TABLET | 50 | | 2 |
| 63940-763-10 | Naproxen Sodium | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63940-763 | NAPROXEN SODIUM TABLET [HARMON STORES INC.] | 2 | Legacy NDC, 2 package rows | 20191218_76a17f69-0071-e102-e053-2991aa0a3a66.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63940-763-05 | 63940076305 | 50 TABLET in 1 BOTTLE (63940-763-05) | 50 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 63940-763-10 | 63940076310 | 100 TABLET in 1 BOTTLE (63940-763-10) | 100 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |