NAPROXEN
- Product NDC
- 70934-124
- 11-digit product format
- 709340124
- Labeler code
- 70934
- Product ID
- 70934-124_b7ae9583-b5b4-97e3-e053-2a95a90a701d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NAPROXEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA091416
- Marketing category
- ANDA
- Marketing start
- 2018-06-06
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-124-20 | 70934012420 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-124-20) | 20 tablet | 2019-03-06 | 0000-00-00 | No | No | Current |
| 70934-124-30 | 70934012430 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-124-30) | 30 tablet | 2018-06-06 | 0000-00-00 | No | No | Current |
| 70934-124-60 | 70934012460 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-124-60) | 60 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 70934-124-90 | 70934012490 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-124-90) | 90 tablet | 2019-02-05 | 0000-00-00 | No | No | Current |