Aleve
- Product NDC
- 0280-0131
- 11-digit product format
- 002800131
- Labeler code
- 0280
- Product ID
- 0280-0131_31bad2d9-c0ba-7f20-e063-6294a90acb17
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAPROXEN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bayer HealthCare LLC.
- Application
- NDA020204
- Marketing category
- NDA
- Marketing start
- 2023-04-04
- 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
- Aleve
- Brand name suffix
- Easy Open Arthritis
- 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, 849728 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0280-0131-01 | AleveEasy Open Arthritis | 200 in 1 BOTTLE | TABLET | 200 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0280-0131-01 | 00280013101 | 200 TABLET in 1 BOTTLE (0280-0131-01) | 200 tablet | 2024-03-25 | No | No | Historical |