Naproxen
- Product NDC
- 50090-4636
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075927
- Marketing category
- ANDA
- Substance
- NAPROXEN
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-4636-0 | 20 TABLET in 1 BOTTLE (50090-4636-0) | 2019-10-22 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| These highlights do not include all the information needed to use NAPROXEN TABLETS safely and effectively. See full prescribing information for NAPROXEN TABLETS. NAPROXEN tablets, for oral use Initial U.S. Approval: 1976 | A-S Medication Solutions | 2023-02-06 | HUMAN PRESCRIPTION DRUG LABEL | 3 |