Naproxen
- Product NDC
- 31722-682
- 11-digit product format
- 317220682
- Labeler code
- 31722
- Product ID
- 31722-682_34759de3-8b17-9ab2-e063-6394a90a6a3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA215776
- Marketing category
- ANDA
- Marketing start
- 2022-06-07
- Substance
- NAPROXEN
- Active strength
- 25 mg/mL
- 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAPROXEN | 25 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 57Y76R9ATQ |
| Rxcui | 311913 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 31722-682-05 | Naproxen | 500 mL in 1 BOTTLE | SUSPENSION | 500 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-682 | NAPROXEN (NAPROXEN) SUSPENSION [CAMBER PHARMACEUTICALS, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250507_fd5e8d84-f92c-4f4b-ab0d-4cda7cf826bd.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 |
|---|
| 31722-682-05 | 31722068205 | 500 mL in 1 BOTTLE (31722-682-05) | 500 ml | 2022-06-07 | 0000-00-00 | No | No | Current |