Naproxen Sodium
- Product NDC
- 49035-762
- 11-digit product format
- 490350762
- Labeler code
- 49035
- Product ID
- 49035-762_4a11d025-58f4-070f-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wal-Mart Stores, Inc.,
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2016-05-25
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 49035-762-10 | Naproxen Sodium | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 49035-762-21 | Naproxen Sodium | 225 in 1 BOTTLE | TABLET | 225 | | 3 |
| 49035-762-24 | Naproxen Sodium | 24 in 1 BOTTLE | TABLET | 24 | | 3 |
| 49035-762-30 | Naproxen Sodium | 300 in 1 BOTTLE | TABLET | 300 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-762 | NAPROXEN SODIUM TABLET [WAL-MART STORES, INC.,] | 3 | Legacy NDC, 4 package rows | 20170503_3d963242-a7b5-1ea4-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49035-762-10 | 49035076210 | 100 in 1 BOTTLE | Historical |
| 49035-762-21 | 49035076221 | 225 in 1 BOTTLE | Historical |
| 49035-762-24 | 49035076224 | 24 in 1 BOTTLE | Historical |
| 49035-762-30 | 49035076230 | 300 in 1 BOTTLE | Historical |