Naproxen Sodium
- Product NDC
- 69848-009
- 11-digit product format
- 698480009
- Labeler code
- 69848
- Product ID
- 69848-009_b96f8277-df52-d3ec-e053-2a95a90afa70
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Granules USA, Inc.
- Application
- ANDA091353
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69848-009-01 | Naproxen Sodium | 10 in 1 BOTTLE | TABLET | 10 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69848-009 | NAPROXEN SODIUM TABLET [GRANULES USA, INC.] | 7 | Legacy NDC, 1 package rows | 20241228_8cb8030c-b281-315c-e053-2a95a90a36f0.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 |
|---|
| 69848-009-01 | 69848000901 | 10 TABLET in 1 BOTTLE (69848-009-01) | 10 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |