Naproxen
- Product NDC
- 72162-2276
- 11-digit product format
- 721622276
- Labeler code
- 72162
- Product ID
- 72162-2276_6d9c5ba4-8d0c-400e-9beb-830a2f9ad85d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091432
- Marketing category
- ANDA
- Marketing start
- 2023-09-10
- 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 |
|---|
| 72162-2276-1 | 72162227601 | 100 TABLET in 1 BOTTLE (72162-2276-1) | 100 tablet | 2024-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Naproxen | Bryant Ranch Prepack | 2025-09-17 | HUMAN PRESCRIPTION DRUG LABEL | 101 |