Naproxen
- Product NDC
- 50090-6667
- 11-digit product format
- 500906667
- Labeler code
- 50090
- Product ID
- 50090-6667_e17033ee-753c-47e7-8fc9-ad0414976874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200429
- Marketing category
- ANDA
- Marketing start
- 2011-11-08
- Substance
- NAPROXEN
- Active strength
- 500 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 57Y76R9ATQ | NAPROXEN | 22204-53-1 | NAPROXEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6667-1 | 50090666701 | 90 TABLET in 1 BOTTLE (50090-6667-1) | 90 tablet | 2023-08-31 | No | No | Historical |
| 50090-6667-2 | 50090666702 | 180 TABLET in 1 BOTTLE (50090-6667-2) | 180 tablet | 2023-08-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Naproxen | A-S Medication Solutions | 2023-09-06 | Human Prescription Drug Label | 1 |