NAPROXEN
- Product NDC
- 61919-173
- 11-digit product format
- 619190173
- Labeler code
- 61919
- Product ID
- 61919-173_9ca98d44-03a8-f379-e053-2995a90a9cb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NAPROXEN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA078250
- Marketing category
- ANDA
- Marketing start
- 2017-05-11
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-173-30 | NAPROXEN | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 61919-173-60 | NAPROXEN | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-173 | NAPROXEN (NAPROXEN SODIUM) TABLET [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20200130_4f4083dc-54fe-109a-e054-00144ff88e88.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 |
|---|
| 61919-173-30 | 61919017330 | 30 TABLET in 1 BOTTLE (61919-173-30) | 30 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |
| 61919-173-60 | 61919017360 | 60 TABLET in 1 BOTTLE (61919-173-60) | 60 tablet | 2017-05-11 | 0000-00-00 | No | No | Current |