naproxen sodium
- Product NDC
- 37808-713
- 11-digit product format
- 378080713
- Labeler code
- 37808
- Product ID
- 37808-713_6ee71bc8-3819-4e08-85f5-9557df90ad5a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2017-10-03
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- naproxen sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAPROXEN SODIUM | 220 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9TN87S3A3C |
| Rxcui | 849574 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-713-79 | naproxen sodium | 400 in 1 BOTTLE | TABLET, FILM COATED | 400 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-713 | NAPROXEN SODIUM TABLET, FILM COATED [H E B] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250308_b5dcf3df-2628-49c7-9d96-64886bebe631.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-713-79 | 37808071379 | 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79) | 2017-10-03 | 0000-00-00 | No | No | Current |