Naproxen Sodium
- Product NDC
- 21130-690
- 11-digit product format
- 211300690
- Labeler code
- 21130
- Product ID
- 21130-690_fe75f23c-9c5e-03a4-e053-6294a90a696d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BETTER LIVING BRANDS LLC.
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2023-06-13
- 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 |
|---|
| 21130-690-05 | Naproxen Sodium | 1 in 1 CARTON | TABLET | 1 | | 2 |
| 21130-690-05 | Naproxen Sodium | 50 in 1 BOTTLE | TABLET | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-690 | NAPROXEN SODIUM TABLET [BETTER LIVING BRANDS LLC.] | 2 | Current NDC, 2 package rows | 20230622_f2c06861-0322-93ed-e053-2995a90a5902.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21130-690-05 | 21130069005 | 1 BOTTLE in 1 CARTON (21130-690-05) / 50 TABLET in 1 BOTTLE | 1 bottle | 2023-06-13 | No | No | Current |