NDC 50844-417-43 - Naproxen Sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50844-417
- Requested NDC
- 50844-417-43
- Package NDCs from labels
- 50844-417-43, 50844-417-22, 50844-417-11, 50844-417-99, 50844-417-98, 50844-417-19, 50844-417-56, 50844-417-14, 50844-417-16
- Manufacturer
- L.N.K. International, Inc. | LNK International, Inc.
- Effective date
- 2026-02-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Quality Plus 44-417 and 44-604 | L.N.K. International, Inc. | LNK International, Inc. | 2026-02-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50844-417-11 | Naproxen Sodium | 60 in 1 CARTON | TABLET, FILM COATED | 60 | 15 | |
| 50844-417-14 | Naproxen Sodium | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | 15 | |
| 50844-417-16 | Naproxen Sodium | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | 15 | |
| 50844-417-19 | Naproxen Sodium | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 15 | |
| 50844-417-19 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 | |
| 50844-417-22 | Naproxen Sodium | 48 in 1 CARTON | TABLET, FILM COATED | 48 | 15 | |
| 50844-417-43 | Naproxen Sodium | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 15 | |
| 50844-417-56 | Naproxen Sodium | 25 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 25 | 15 | |
| 50844-417-98 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 | |
| 50844-417-99 | Naproxen Sodium | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 15 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.